Canonical Allele Identifier: CA2677953679

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354421-C-CGAA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354421_31354422insGAA , CM000668.2:g.31354421_31354422insGAA	GRCh38
NC_000006.11:g.31322198_31322199insGAA , CM000668.1:g.31322198_31322199insGAA	GRCh37
NC_000006.10:g.31430177_31430178insGAA	NCBI36
NG_023187.1:g.7791_7792insTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3140+57_3140+58insTTC
ENST00000481849.6:n.3100+57_3100+58insTTC
ENST00000497377.6:n.3007+57_3007+58insTTC
ENST00000696558.1:c.1162+57_1162+58insTTC	ENSP00000512716.1:n.1162+57_1162+58insTTC
ENST00000696559.1:c.*4+57_*4+58insTTC	ENSP00000512717.1:n.*4+57_*4+58insTTC
ENST00000696560.1:c.*4+57_*4+58insTTC	ENSP00000512718.1:n.*4+57_*4+58insTTC
ENST00000696561.1:c.*4+57_*4+58insTTC	ENSP00000512719.1:n.*4+57_*4+58insTTC
ENST00000696562.1:c.*4+57_*4+58insTTC	ENSP00000512720.1:n.*4+57_*4+58insTTC
ENST00000412585.7:c.*4+57_*4+58insTTC MANE Select	ENSP00000399168.2:n.*4+57_*4+58insTTC
ENST00000412585.6:c.*4+57_*4+58insTTC	ENSP00000399168.2:n.*4+57_*4+58insTTC
ENST00000481849.5:n.328+57_328+58insTTC
ENST00000497377.5:n.492+57_492+58insTTC
NM_005514.6:c.*4+57_*4+58insTTC	NP_005505.2:n.*4+57_*4+58insTTC
XM_011514556.1:c.*4+57_*4+58insTTC	XP_011512858.1:n.*4+57_*4+58insTTC
XM_011514557.1:c.*4+57_*4+58insTTC	XP_011512859.1:n.*4+57_*4+58insTTC
XR_926175.1:n.1532+57_1532+58insTTC
NM_005514.7:c.*4+57_*4+58insTTC	NP_005505.2:n.*4+57_*4+58insTTC
NM_005514.8:c.*4+57_*4+58insTTC MANE Select	NP_005505.2:n.*4+57_*4+58insTTC