Canonical Allele Identifier: CA12829676

Gene: BLK

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11495032T>C , CM000670.2:g.11495032T>C	GRCh38
NC_000008.10:g.11352541T>C , CM000670.1:g.11352541T>C	GRCh37
NC_000008.9:g.11389950T>C	NCBI36
NG_023543.1:g.6021T>C
NG_023543.2:g.6021T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.274+7865T>C
ENST00000696154.1:c.-91+7865T>C	ENSP00000512445.1:n.-91+7865T>C
ENST00000259089.9:c.-2+441T>C MANE Select	ENSP00000259089.4:n.-2+441T>C
ENST00000645242.1:c.-91+7865T>C	ENSP00000494690.1:n.-91+7865T>C
ENST00000259089.8:c.-2+441T>C	ENSP00000259089.4:n.-2+441T>C
ENST00000525389.1:n.423+441T>C
ENST00000529894.1:c.-91+441T>C	ENSP00000433663.1:n.-91+441T>C
NM_001715.2:c.-2+441T>C	NP_001706.2:n.-2+441T>C
XM_011543824.1:c.-2+441T>C	XP_011542126.1:n.-2+441T>C
XM_011543827.1:c.-91+441T>C	XP_011542129.1:n.-91+441T>C
XM_011543828.1:c.-2+441T>C	XP_011542130.1:n.-2+441T>C
XM_011543829.1:c.-2+441T>C	XP_011542131.1:n.-2+441T>C
NM_001330465.1:c.-91+441T>C	NP_001317394.1:n.-91+441T>C
XM_011543828.3:c.-2+441T>C	XP_011542130.1:n.-2+441T>C
XM_011543829.3:c.-2+441T>C	XP_011542131.1:n.-2+441T>C
NM_001715.3:c.-2+441T>C MANE Select	NP_001706.2:n.-2+441T>C
NM_001330465.2:c.-91+441T>C	NP_001317394.1:n.-91+441T>C