Canonical Allele Identifier: CA370316968

Gene: BLK

Linked Data

• gnomAD v4: 8-11564044-T-C
• MyVariant Identifiers: chr8:g.11421553T>C (hg19) ; chr8:g.11564044T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564044T>C , CM000670.2:g.11564044T>C	GRCh38
NC_000008.10:g.11421553T>C , CM000670.1:g.11421553T>C	GRCh37
NC_000008.9:g.11458962T>C	NCBI36
NG_023543.1:g.75033T>C
NG_023543.2:g.75033T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1562T>C
ENST00000696154.1:c.*772T>C	ENSP00000512445.1:n.*772T>C
ENST00000696155.1:n.338T>C
ENST00000259089.9:c.1454T>C MANE Select	ENSP00000259089.4:p.Phe485Ser
ENST00000645242.1:c.1241T>C	ENSP00000494690.1:p.Phe414Ser
ENST00000259089.8:c.1454T>C	ENSP00000259089.4:p.Phe485Ser
ENST00000526097.1:n.1394T>C
ENST00000529894.1:c.1241T>C	ENSP00000433663.1:p.Phe414Ser
NM_001715.2:c.1454T>C	NP_001706.2:p.Phe485Ser
XM_011543824.1:c.1532T>C	XP_011542126.1:p.Phe511Ser
XM_011543825.1:c.1532T>C	XP_011542127.1:p.Phe511Ser
XM_011543826.1:c.1532T>C	XP_011542128.1:p.Phe511Ser
XM_011543827.1:c.1319T>C	XP_011542129.1:p.Phe440Ser
NM_001330465.1:c.1241T>C	NP_001317394.1:p.Phe414Ser
XM_011543825.3:c.1532T>C	XP_011542127.1:p.Phe511Ser
NM_001715.3:c.1454T>C MANE Select	NP_001706.2:p.Phe485Ser
NM_001330465.2:c.1241T>C	NP_001317394.1:p.Phe414Ser