Canonical Allele Identifier: CA370316921

Gene: BLK

Linked Data

• gnomAD v4: 8-11564031-C-A
• MyVariant Identifiers: chr8:g.11421540C>A (hg19) ; chr8:g.11564031C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564031C>A , CM000670.2:g.11564031C>A	GRCh38
NC_000008.10:g.11421540C>A , CM000670.1:g.11421540C>A	GRCh37
NC_000008.9:g.11458949C>A	NCBI36
NG_023543.1:g.75020C>A
NG_023543.2:g.75020C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1549C>A
ENST00000696154.1:c.*759C>A	ENSP00000512445.1:n.*759C>A
ENST00000696155.1:n.325C>A
ENST00000259089.9:c.1441C>A MANE Select	ENSP00000259089.4:p.Pro481Thr
ENST00000645242.1:c.1228C>A	ENSP00000494690.1:p.Pro410Thr
ENST00000259089.8:c.1441C>A	ENSP00000259089.4:p.Pro481Thr
ENST00000526097.1:n.1381C>A
ENST00000529894.1:c.1228C>A	ENSP00000433663.1:p.Pro410Thr
NM_001715.2:c.1441C>A	NP_001706.2:p.Pro481Thr
XM_011543824.1:c.1519C>A	XP_011542126.1:p.Pro507Thr
XM_011543825.1:c.1519C>A	XP_011542127.1:p.Pro507Thr
XM_011543826.1:c.1519C>A	XP_011542128.1:p.Pro507Thr
XM_011543827.1:c.1306C>A	XP_011542129.1:p.Pro436Thr
NM_001330465.1:c.1228C>A	NP_001317394.1:p.Pro410Thr
XM_011543825.3:c.1519C>A	XP_011542127.1:p.Pro507Thr
NM_001715.3:c.1441C>A MANE Select	NP_001706.2:p.Pro481Thr
NM_001330465.2:c.1228C>A	NP_001317394.1:p.Pro410Thr