Canonical Allele Identifier: CA2677957596

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356691-C-CCCAGGT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356692_31356693insCAGGTC , CM000668.2:g.31356692_31356693insCAGGTC	GRCh38
NC_000006.11:g.31324469_31324470insCAGGTC , CM000668.1:g.31324469_31324470insCAGGTC	GRCh37
NC_000006.10:g.31432448_31432449insCAGGTC	NCBI36
NG_023187.1:g.5521_5522insACCTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1812_1813insACCTGG
ENST00000481849.6:n.1812_1813insACCTGG
ENST00000497377.6:n.1812_1813insACCTGG
ENST00000640094.2:c.339_340insACCTGG	ENSP00000491275.2:p.Glu113_Ala114insThrTrp
ENST00000696558.1:c.339_340insACCTGG	ENSP00000512716.1:p.Glu113_Ala114insThrTrp
ENST00000696559.1:c.339_340insACCTGG	ENSP00000512717.1:p.Glu113_Ala114insThrTrp
ENST00000696560.1:c.339_340insACCTGG	ENSP00000512718.1:p.Glu113_Ala114insThrTrp
ENST00000696561.1:c.339_340insACCTGG	ENSP00000512719.1:p.Glu113_Ala114insThrTrp
ENST00000696562.1:c.339_340insACCTGG	ENSP00000512720.1:p.Glu113_Ala114insThrTrp
ENST00000412585.7:c.339_340insACCTGG MANE Select	ENSP00000399168.2:p.Glu113_Ala114insThrTrp
ENST00000412585.6:c.339_340insACCTGG	ENSP00000399168.2:p.Glu113_Ala114insThrTrp
ENST00000434333.1:c.372_373insACCTGG	ENSP00000405931.1:p.Glu124_Ala125insThrTrp
ENST00000474381.1:n.214_215insACCTGG
ENST00000498007.1:n.360_361insACCTGG
ENST00000603274.1:n.46_47insCAGGTC
NM_005514.6:c.339_340insACCTGG	NP_005505.2:p.Glu113_Ala114insThrTrp
XM_011514556.1:c.372_373insACCTGG	XP_011512858.1:p.Glu124_Ala125insThrTrp
XM_011514557.1:c.339_340insACCTGG	XP_011512859.1:p.Glu113_Ala114insThrTrp
XR_926175.1:n.349_350insACCTGG
NM_005514.7:c.339_340insACCTGG	NP_005505.2:p.Glu113_Ala114insThrTrp
NM_005514.8:c.339_340insACCTGG MANE Select	NP_005505.2:p.Glu113_Ala114insThrTrp