Canonical Allele Identifier: CA370316728

Gene: BLK

Linked Data

• MyVariant Identifiers: chr8:g.11421480C>T (hg19) ; chr8:g.11563971C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11563971C>T , CM000670.2:g.11563971C>T	GRCh38
NC_000008.10:g.11421480C>T , CM000670.1:g.11421480C>T	GRCh37
NC_000008.9:g.11458889C>T	NCBI36
NG_023543.1:g.74960C>T
NG_023543.2:g.74960C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1489C>T
ENST00000696154.1:c.*699C>T	ENSP00000512445.1:n.*699C>T
ENST00000696155.1:n.265C>T
ENST00000259089.9:c.1381C>T MANE Select	ENSP00000259089.4:p.Pro461Ser
ENST00000645242.1:c.1168C>T	ENSP00000494690.1:p.Pro390Ser
ENST00000259089.8:c.1381C>T	ENSP00000259089.4:p.Pro461Ser
ENST00000526097.1:n.1321C>T
ENST00000529894.1:c.1168C>T	ENSP00000433663.1:p.Pro390Ser
NM_001715.2:c.1381C>T	NP_001706.2:p.Pro461Ser
XM_011543824.1:c.1459C>T	XP_011542126.1:p.Pro487Ser
XM_011543825.1:c.1459C>T	XP_011542127.1:p.Pro487Ser
XM_011543826.1:c.1459C>T	XP_011542128.1:p.Pro487Ser
XM_011543827.1:c.1246C>T	XP_011542129.1:p.Pro416Ser
NM_001330465.1:c.1168C>T	NP_001317394.1:p.Pro390Ser
XM_011543825.3:c.1459C>T	XP_011542127.1:p.Pro487Ser
NM_001715.3:c.1381C>T MANE Select	NP_001706.2:p.Pro461Ser
NM_001330465.2:c.1168C>T	NP_001317394.1:p.Pro390Ser