Canonical Allele Identifier: CA2677956943

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356432-G-GCCAC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356432_31356433insCCAC , CM000668.2:g.31356432_31356433insCCAC	GRCh38
NC_000006.11:g.31324209_31324210insCCAC , CM000668.1:g.31324209_31324210insCCAC	GRCh37
NC_000006.10:g.31432188_31432189insCCAC	NCBI36
NG_023187.1:g.5780_5781insGTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1826_1827insGTGG
ENST00000481849.6:n.1826_1827insGTGG
ENST00000497377.6:n.1826_1827insGTGG
ENST00000640094.2:c.353_354insGTGG	ENSP00000491275.2:p.Leu119TrpfsTer21
ENST00000696558.1:c.353_354insGTGG	ENSP00000512716.1:p.Leu119TrpfsTer21
ENST00000696559.1:c.353_354insGTGG	ENSP00000512717.1:p.Leu119TrpfsTer21
ENST00000696560.1:c.353_354insGTGG	ENSP00000512718.1:p.Leu119TrpfsTer21
ENST00000696561.1:c.353_354insGTGG	ENSP00000512719.1:p.Leu119TrpfsTer21
ENST00000696562.1:c.353_354insGTGG	ENSP00000512720.1:p.Leu119TrpfsTer21
ENST00000412585.7:c.353_354insGTGG MANE Select	ENSP00000399168.2:p.Leu119TrpfsTer21
ENST00000412585.6:c.353_354insGTGG	ENSP00000399168.2:p.Leu119TrpfsTer21
ENST00000434333.1:c.386_387insGTGG	ENSP00000405931.1:p.Leu130TrpfsTer21
ENST00000474381.1:n.228_229insGTGG
ENST00000498007.1:n.619_620insGTGG
NM_005514.6:c.353_354insGTGG	NP_005505.2:p.Leu119TrpfsTer21
XM_011514556.1:c.386_387insGTGG	XP_011512858.1:p.Leu130TrpfsTer21
XM_011514557.1:c.353_354insGTGG	XP_011512859.1:p.Leu119TrpfsTer21
XR_926175.1:n.363_364insGTGG
NM_005514.7:c.353_354insGTGG	NP_005505.2:p.Leu119TrpfsTer21
NM_005514.8:c.353_354insGTGG MANE Select	NP_005505.2:p.Leu119TrpfsTer21