Canonical Allele Identifier: CA370316798

Gene: BLK

Linked Data

• MyVariant Identifiers: chr8:g.11421502T>C (hg19) ; chr8:g.11563993T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11563993T>C , CM000670.2:g.11563993T>C	GRCh38
NC_000008.10:g.11421502T>C , CM000670.1:g.11421502T>C	GRCh37
NC_000008.9:g.11458911T>C	NCBI36
NG_023543.1:g.74982T>C
NG_023543.2:g.74982T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1511T>C
ENST00000696154.1:c.*721T>C	ENSP00000512445.1:n.*721T>C
ENST00000696155.1:n.287T>C
ENST00000259089.9:c.1403T>C MANE Select	ENSP00000259089.4:p.Val468Ala
ENST00000645242.1:c.1190T>C	ENSP00000494690.1:p.Val397Ala
ENST00000259089.8:c.1403T>C	ENSP00000259089.4:p.Val468Ala
ENST00000526097.1:n.1343T>C
ENST00000529894.1:c.1190T>C	ENSP00000433663.1:p.Val397Ala
NM_001715.2:c.1403T>C	NP_001706.2:p.Val468Ala
XM_011543824.1:c.1481T>C	XP_011542126.1:p.Val494Ala
XM_011543825.1:c.1481T>C	XP_011542127.1:p.Val494Ala
XM_011543826.1:c.1481T>C	XP_011542128.1:p.Val494Ala
XM_011543827.1:c.1268T>C	XP_011542129.1:p.Val423Ala
NM_001330465.1:c.1190T>C	NP_001317394.1:p.Val397Ala
XM_011543825.3:c.1481T>C	XP_011542127.1:p.Val494Ala
NM_001715.3:c.1403T>C MANE Select	NP_001706.2:p.Val468Ala
NM_001330465.2:c.1190T>C	NP_001317394.1:p.Val397Ala