Canonical Allele Identifier: CA1279175104

Gene: BCL2L11

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111150685G>T , CM000664.2:g.111150685G>T	GRCh38
NC_000002.11:g.111908262G>T , CM000664.1:g.111908262G>T	GRCh37
NC_000002.10:g.111624733G>T	NCBI36
NG_029006.1:g.34772G>T , LRG_620:g.34772G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393252.4:c.780+538G>T	ENSP00000376941.4:n.780+538G>T
ENST00000433098.6:c.561+538G>T	ENSP00000401662.2:n.561+538G>T
ENST00000393256.8:c.498+538G>T MANE Select	ENSP00000376943.2:n.498+538G>T
ENST00000308659.12:c.318+538G>T	ENSP00000309226.8:n.318+538G>T
ENST00000361493.10:c.344+538G>T	ENSP00000354879.6:n.344+538G>T
ENST00000393256.7:c.498+538G>T	ENSP00000376943.2:n.498+538G>T
ENST00000415458.5:c.215-3095G>T	ENSP00000393781.1:n.215-3095G>T
ENST00000431217.1:c.531+538G>T	ENSP00000394640.1:n.531+538G>T
ENST00000433098.5:c.318+538G>T	ENSP00000401662.1:n.318+538G>T
ENST00000436733.5:c.395-3095G>T	ENSP00000403727.1:n.395-3095G>T
ENST00000437029.5:c.498+538G>T	ENSP00000412892.1:n.498+538G>T
ENST00000439718.1:c.228+538G>T	ENSP00000411137.1:n.228+538G>T
ENST00000452231.5:c.228+538G>T	ENSP00000391292.1:n.228+538G>T
ENST00000610735.4:c.395-3095G>T	ENSP00000481030.1:n.395-3095G>T
ENST00000615946.4:c.228+538G>T	ENSP00000481423.1:n.228+538G>T
ENST00000619294.4:c.*123+538G>T	ENSP00000479714.1:n.*123+538G>T
ENST00000620862.4:c.318+538G>T	ENSP00000478133.1:n.318+538G>T
ENST00000621302.4:c.498+538G>T	ENSP00000481652.1:n.498+538G>T
ENST00000622509.4:c.498+538G>T	ENSP00000482175.1:n.498+538G>T
ENST00000622612.4:c.395-13448G>T	ENSP00000484360.1:n.395-13448G>T
NM_001204106.1:c.228+538G>T	NP_001191035.1:n.228+538G>T
NM_001204107.1:c.228+538G>T , LRG_620t1:c.228+538G>T	NP_001191036.1:n.228+538G>T
NM_001204108.1:c.498+538G>T , LRG_620t2:c.498+538G>T	NP_001191037.1:n.498+538G>T
NM_001204109.1:c.395-3095G>T	NP_001191038.1:n.395-3095G>T
NM_001204110.1:c.228+538G>T	NP_001191039.1:n.228+538G>T
NM_001204111.1:c.215-13448G>T	NP_001191040.1:n.215-13448G>T
NM_001204112.1:c.215-3095G>T	NP_001191041.1:n.215-3095G>T
NM_006538.4:c.318+538G>T	NP_006529.1:n.318+538G>T
NM_138621.4:c.498+538G>T	NP_619527.1:n.498+538G>T
NM_138622.3:c.498+538G>T	NP_619528.1:n.498+538G>T
NM_138623.3:c.318+538G>T	NP_619529.1:n.318+538G>T
NM_138624.3:c.*123+538G>T	NP_619530.1:n.*123+538G>T
NM_138625.3:c.*116+538G>T , LRG_620t4:c.*116+538G>T	NP_619531.1:n.*116+538G>T
NM_138626.3:c.395-13448G>T	NP_619532.1:n.395-13448G>T
NM_138627.3:c.125-13448G>T	NP_619533.1:n.125-13448G>T
NM_207003.2:c.228+538G>T	NP_996886.1:n.228+538G>T
XM_005263550.2:c.*415G>T	XP_005263607.1:n.*415G>T
XM_005263551.1:c.780+538G>T	XP_005263608.1:n.780+538G>T
XM_005263552.2:c.*415G>T	XP_005263609.1:n.*415G>T
XM_005263553.1:c.600+538G>T	XP_005263610.1:n.600+538G>T
XM_005263554.1:c.677-13448G>T	XP_005263611.1:n.677-13448G>T
XM_005263555.2:c.*415G>T	XP_005263612.1:n.*415G>T
XM_005263556.2:c.*415G>T	XP_005263613.1:n.*415G>T
XM_005263557.3:c.*415G>T	XP_005263614.1:n.*415G>T
XM_005263559.1:c.510+538G>T	XP_005263616.1:n.510+538G>T
XM_005263561.2:c.*415G>T	XP_005263618.1:n.*415G>T
XM_011510463.1:c.*415G>T	XP_011508765.1:n.*415G>T
XR_244801.1:n.839+538G>T
XR_244802.2:n.839+538G>T
XR_922828.1:n.839+538G>T
XR_922829.1:n.839+538G>T
XR_922830.1:n.736-3095G>T
XM_005263550.4:c.*415G>T	XP_005263607.1:n.*415G>T
XM_005263551.3:c.780+538G>T	XP_005263608.1:n.780+538G>T
XM_005263552.4:c.*415G>T	XP_005263609.1:n.*415G>T
XM_005263553.3:c.600+538G>T	XP_005263610.1:n.600+538G>T
XM_005263554.3:c.677-13448G>T	XP_005263611.1:n.677-13448G>T
XM_005263555.4:c.*415G>T	XP_005263612.1:n.*415G>T
XM_005263556.3:c.*415G>T	XP_005263613.1:n.*415G>T
XM_005263557.4:c.*415G>T	XP_005263614.1:n.*415G>T
XM_005263559.3:c.510+538G>T	XP_005263616.1:n.510+538G>T
XM_005263561.3:c.*415G>T	XP_005263618.1:n.*415G>T
XM_017003101.2:c.497-13448G>T	XP_016858590.1:n.497-13448G>T
XM_017003102.1:c.*415G>T	XP_016858591.1:n.*415G>T
XR_001738579.2:n.873+538G>T
XR_001738580.2:n.660+538G>T
XR_002958776.1:n.677+538G>T
XR_244801.3:n.840+538G>T
XR_922828.3:n.840+538G>T
XR_922829.3:n.840+538G>T
NM_138621.5:c.498+538G>T MANE Select	NP_619527.1:n.498+538G>T
NM_001204106.2:c.228+538G>T	NP_001191035.1:n.228+538G>T
NM_001204110.2:c.228+538G>T	NP_001191039.1:n.228+538G>T
NM_001204111.2:c.215-13448G>T	NP_001191040.1:n.215-13448G>T
NM_001204112.2:c.215-3095G>T	NP_001191041.1:n.215-3095G>T
NM_006538.5:c.318+538G>T	NP_006529.1:n.318+538G>T
NM_138625.4:c.*116+538G>T	NP_619531.1:n.*116+538G>T
NM_138627.4:c.125-13448G>T	NP_619533.1:n.125-13448G>T
NM_207003.3:c.228+538G>T	NP_996886.1:n.228+538G>T
NM_001204109.2:c.395-3095G>T	NP_001191038.1:n.395-3095G>T
NM_138622.4:c.498+538G>T	NP_619528.1:n.498+538G>T
NM_138623.4:c.318+538G>T	NP_619529.1:n.318+538G>T
NM_138624.4:c.*123+538G>T	NP_619530.1:n.*123+538G>T
NM_138626.4:c.395-13448G>T	NP_619532.1:n.395-13448G>T