Canonical Allele Identifier: CA2838139393
Gene: HLA-B HGNC NCBI

Linked Data

MutSpliceDB: CA2838139393

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356686_31356687delinsGA , CM000668.2:g.31356686_31356687delinsGA GRCh38
NC_000006.11:g.31324463_31324464delinsGA , CM000668.1:g.31324463_31324464delinsGA GRCh37
NC_000006.10:g.31432442_31432443delinsGA NCBI36
NG_023187.1:g.5526_5527delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1816+1_1816+2delinsTC
ENST00000481849.6:n.1816+1_1816+2delinsTC
ENST00000497377.6:n.1816+1_1816+2delinsTC
ENST00000640094.2:c.343+1_343+2delinsTC ENSP00000491275.2:n.343+1_343+2delinsTC
ENST00000696558.1:c.343+1_343+2delinsTC ENSP00000512716.1:n.343+1_343+2delinsTC
ENST00000696559.1:c.343+1_343+2delinsTC ENSP00000512717.1:n.343+1_343+2delinsTC
ENST00000696560.1:c.343+1_343+2delinsTC ENSP00000512718.1:n.343+1_343+2delinsTC
ENST00000696561.1:c.343+1_343+2delinsTC ENSP00000512719.1:n.343+1_343+2delinsTC
ENST00000696562.1:c.343+1_343+2delinsTC ENSP00000512720.1:n.343+1_343+2delinsTC
ENST00000412585.7:c.343+1_343+2delinsTC MANE Select ENSP00000399168.2:n.343+1_343+2delinsTC
ENST00000412585.6:c.343+1_343+2delinsTC ENSP00000399168.2:n.343+1_343+2delinsTC
ENST00000434333.1:c.376+1_376+2delinsTC ENSP00000405931.1:n.376+1_376+2delinsTC
ENST00000474381.1:n.218+1_218+2delinsTC
ENST00000498007.1:n.365_366delinsTC
ENST00000603274.1:n.40_41delinsGA
NM_005514.6:c.343+1_343+2delinsTC NP_005505.2:n.343+1_343+2delinsTC
XM_011514556.1:c.376+1_376+2delinsTC XP_011512858.1:n.376+1_376+2delinsTC
XM_011514557.1:c.343+1_343+2delinsTC XP_011512859.1:n.343+1_343+2delinsTC
XR_926175.1:n.353+1_353+2delinsTC
NM_005514.7:c.343+1_343+2delinsTC NP_005505.2:n.343+1_343+2delinsTC
NM_005514.8:c.343+1_343+2delinsTC MANE Select NP_005505.2:n.343+1_343+2delinsTC