Canonical Allele Identifier: CA348352670

Gene: BCL2L11

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111135407A>T , CM000664.2:g.111135407A>T	GRCh38
NC_000002.11:g.111892984A>T , CM000664.1:g.111892984A>T	GRCh37
NC_000002.10:g.111609455A>T	NCBI36
NG_029006.1:g.19494A>T , LRG_620:g.19494A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393252.4:c.676+11268A>T	ENSP00000376941.4:n.676+11268A>T
ENST00000433098.6:c.457+11268A>T	ENSP00000401662.2:n.457+11268A>T
ENST00000438054.2:c.215-6906A>T	ENSP00000389225.2:n.215-6906A>T
ENST00000393256.8:c.394+11268A>T MANE Select	ENSP00000376943.2:n.394+11268A>T
ENST00000308659.12:c.214+11268A>T	ENSP00000309226.8:n.214+11268A>T
ENST00000357757.6:c.215-6906A>T	ENSP00000350398.3:n.215-6906A>T
ENST00000361493.10:c.240+5160A>T	ENSP00000354879.6:n.240+5160A>T
ENST00000393256.7:c.394+11268A>T	ENSP00000376943.2:n.394+11268A>T
ENST00000415458.5:c.214+11268A>T	ENSP00000393781.1:n.214+11268A>T
ENST00000431217.1:c.395-9081A>T	ENSP00000394640.1:n.395-9081A>T
ENST00000433098.5:c.214+11268A>T	ENSP00000401662.1:n.214+11268A>T
ENST00000436733.5:c.394+11268A>T	ENSP00000403727.1:n.394+11268A>T
ENST00000437029.5:c.394+11268A>T	ENSP00000412892.1:n.394+11268A>T
ENST00000438054.1:c.209-6906A>T	ENSP00000389225.1:n.209-6906A>T
ENST00000439718.1:c.124+11538A>T	ENSP00000411137.1:n.124+11538A>T
ENST00000452231.5:c.124+11538A>T	ENSP00000391292.1:n.124+11538A>T
ENST00000610735.4:c.394+11268A>T	ENSP00000481030.1:n.394+11268A>T
ENST00000615946.4:c.124+11538A>T	ENSP00000481423.1:n.124+11538A>T
ENST00000619294.4:c.395-9081A>T	ENSP00000479714.1:n.395-9081A>T
ENST00000620862.4:c.214+11268A>T	ENSP00000478133.1:n.214+11268A>T
ENST00000621302.4:c.394+11268A>T	ENSP00000481652.1:n.394+11268A>T
ENST00000622509.4:c.394+11268A>T	ENSP00000482175.1:n.394+11268A>T
ENST00000622612.4:c.394+11268A>T	ENSP00000484360.1:n.394+11268A>T
NM_001204106.1:c.124+11538A>T	NP_001191035.1:n.124+11538A>T
NM_001204107.1:c.124+11538A>T , LRG_620t1:c.124+11538A>T	NP_001191036.1:n.124+11538A>T
NM_001204108.1:c.394+11268A>T , LRG_620t2:c.394+11268A>T	NP_001191037.1:n.394+11268A>T
NM_001204109.1:c.394+11268A>T	NP_001191038.1:n.394+11268A>T
NM_001204110.1:c.124+11538A>T	NP_001191039.1:n.124+11538A>T
NM_001204111.1:c.214+11268A>T	NP_001191040.1:n.214+11268A>T
NM_001204112.1:c.214+11268A>T	NP_001191041.1:n.214+11268A>T
NM_001204113.1:c.215-6906A>T , LRG_620t3:c.215-6906A>T	NP_001191042.1:n.215-6906A>T
NM_006538.4:c.214+11268A>T	NP_006529.1:n.214+11268A>T
NM_138621.4:c.394+11268A>T	NP_619527.1:n.394+11268A>T
NM_138622.3:c.394+11268A>T	NP_619528.1:n.394+11268A>T
NM_138623.3:c.214+11268A>T	NP_619529.1:n.214+11268A>T
NM_138624.3:c.395-9081A>T	NP_619530.1:n.395-9081A>T
NM_138625.3:c.*12+5160A>T , LRG_620t4:c.*12+5160A>T	NP_619531.1:n.*12+5160A>T
NM_138626.3:c.394+11268A>T	NP_619532.1:n.394+11268A>T
NM_138627.3:c.124+11538A>T	NP_619533.1:n.124+11538A>T
NM_207003.2:c.124+11538A>T	NP_996886.1:n.124+11538A>T
XM_005263550.2:c.676+11268A>T	XP_005263607.1:n.676+11268A>T
XM_005263551.1:c.676+11268A>T	XP_005263608.1:n.676+11268A>T
XM_005263552.2:c.496+11268A>T	XP_005263609.1:n.496+11268A>T
XM_005263553.1:c.496+11268A>T	XP_005263610.1:n.496+11268A>T
XM_005263554.1:c.676+11268A>T	XP_005263611.1:n.676+11268A>T
XM_005263555.2:c.406+11538A>T	XP_005263612.1:n.406+11538A>T
XM_005263556.2:c.394+11268A>T	XP_005263613.1:n.394+11268A>T
XM_005263557.3:c.394+11268A>T	XP_005263614.1:n.394+11268A>T
XM_005263559.1:c.406+11538A>T	XP_005263616.1:n.406+11538A>T
XM_005263561.2:c.214+11268A>T	XP_005263618.1:n.214+11268A>T
XM_011510462.1:c.677-6906A>T	XP_011508764.1:n.677-6906A>T
XM_011510463.1:c.445+11268A>T	XP_011508765.1:n.445+11268A>T
XM_011510465.1:c.497-6906A>T	XP_011508767.1:n.497-6906A>T
XR_244801.1:n.735+11268A>T
XR_244802.2:n.735+11268A>T
XR_922828.1:n.735+11268A>T
XR_922829.1:n.735+11268A>T
XR_922830.1:n.735+11268A>T
XM_005263550.4:c.676+11268A>T	XP_005263607.1:n.676+11268A>T
XM_005263551.3:c.676+11268A>T	XP_005263608.1:n.676+11268A>T
XM_005263552.4:c.496+11268A>T	XP_005263609.1:n.496+11268A>T
XM_005263553.3:c.496+11268A>T	XP_005263610.1:n.496+11268A>T
XM_005263554.3:c.676+11268A>T	XP_005263611.1:n.676+11268A>T
XM_005263555.4:c.406+11538A>T	XP_005263612.1:n.406+11538A>T
XM_005263556.3:c.394+11268A>T	XP_005263613.1:n.394+11268A>T
XM_005263557.4:c.394+11268A>T	XP_005263614.1:n.394+11268A>T
XM_005263559.3:c.406+11538A>T	XP_005263616.1:n.406+11538A>T
XM_005263561.3:c.214+11268A>T	XP_005263618.1:n.214+11268A>T
XM_017003101.2:c.496+11268A>T	XP_016858590.1:n.496+11268A>T
XM_017003102.1:c.124+11538A>T	XP_016858591.1:n.124+11538A>T
XR_001738579.2:n.737-9081A>T
XR_001738580.2:n.556+11268A>T
XR_002958776.1:n.573+11268A>T
XR_244801.3:n.736+11268A>T
XR_922828.3:n.736+11268A>T
XR_922829.3:n.736+11268A>T
NM_138621.5:c.394+11268A>T MANE Select	NP_619527.1:n.394+11268A>T
NM_001204106.2:c.124+11538A>T	NP_001191035.1:n.124+11538A>T
NM_001204110.2:c.124+11538A>T	NP_001191039.1:n.124+11538A>T
NM_001204111.2:c.214+11268A>T	NP_001191040.1:n.214+11268A>T
NM_001204112.2:c.214+11268A>T	NP_001191041.1:n.214+11268A>T
NM_006538.5:c.214+11268A>T	NP_006529.1:n.214+11268A>T
NM_138625.4:c.*12+5160A>T	NP_619531.1:n.*12+5160A>T
NM_138627.4:c.124+11538A>T	NP_619533.1:n.124+11538A>T
NM_207003.3:c.124+11538A>T	NP_996886.1:n.124+11538A>T
NM_001204109.2:c.394+11268A>T	NP_001191038.1:n.394+11268A>T
NM_138622.4:c.394+11268A>T	NP_619528.1:n.394+11268A>T
NM_138623.4:c.214+11268A>T	NP_619529.1:n.214+11268A>T
NM_138624.4:c.395-9081A>T	NP_619530.1:n.395-9081A>T
NM_138626.4:c.394+11268A>T	NP_619532.1:n.394+11268A>T