Canonical Allele Identifier: CA2642093029

Gene: BCL2

Linked Data

• gnomAD v4: 18-63318887-CTTTATTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63318888_63318894del , CM000680.2:g.63318888_63318894del	GRCh38
NC_000018.9:g.60986121_60986127del , CM000680.1:g.60986121_60986127del	GRCh37
NC_000018.8:g.59137101_59137107del	NCBI36
NG_009361.1:g.5487_5493del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333681.5:c.-228_-222del MANE Select	ENSP00000329623.3:n.-228_-222del
ENST00000333681.4:c.-228_-222del	ENSP00000329623.3:n.-228_-222del
ENST00000398117.1:c.-228_-222del	ENSP00000381185.1:n.-228_-222del
NM_000633.2:c.-228_-222del	NP_000624.2:n.-228_-222del
NM_000657.2:c.-228_-222del	NP_000648.2:n.-228_-222del
XM_011526135.1:c.-228_-222del	XP_011524437.1:n.-228_-222del
XR_935246.1:n.885_891del
XR_935247.1:n.885_891del
XR_935248.1:n.664_670del
XM_011526135.3:c.-228_-222del	XP_011524437.1:n.-228_-222del
XM_017025917.2:c.-228_-222del	XP_016881406.1:n.-228_-222del
XR_935248.3:n.1166_1172del
NM_000633.3:c.-228_-222del MANE Select	NP_000624.2:n.-228_-222del
NM_000657.3:c.-228_-222del	NP_000648.2:n.-228_-222del