Canonical Allele Identifier: CA2677957721
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356763_31356764insTTT , CM000668.2:g.31356763_31356764insTTT GRCh38
NC_000006.11:g.31324540_31324541insTTT , CM000668.1:g.31324540_31324541insTTT GRCh37
NC_000006.10:g.31432519_31432520insTTT NCBI36
NG_023187.1:g.5450_5451insAAA

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1741_1742insAAA
ENST00000481849.6:n.1741_1742insAAA
ENST00000497377.6:n.1741_1742insAAA
ENST00000640094.2:c.268_269insAAA ENSP00000491275.2:p.Gln89_Ile90insLys
ENST00000696558.1:c.268_269insAAA ENSP00000512716.1:p.Gln89_Ile90insLys
ENST00000696559.1:c.268_269insAAA ENSP00000512717.1:p.Gln89_Ile90insLys
ENST00000696560.1:c.268_269insAAA ENSP00000512718.1:p.Gln89_Ile90insLys
ENST00000696561.1:c.268_269insAAA ENSP00000512719.1:p.Gln89_Ile90insLys
ENST00000696562.1:c.268_269insAAA ENSP00000512720.1:p.Gln89_Ile90insLys
ENST00000412585.7:c.268_269insAAA MANE Select ENSP00000399168.2:p.Gln89_Ile90insLys
ENST00000412585.6:c.268_269insAAA ENSP00000399168.2:p.Gln89_Ile90insLys
ENST00000434333.1:c.301_302insAAA ENSP00000405931.1:p.Gln100_Ile101insLys
ENST00000474381.1:n.143_144insAAA
ENST00000498007.1:n.289_290insAAA
ENST00000603274.1:n.117_118insTTT
NM_005514.6:c.268_269insAAA NP_005505.2:p.Gln89_Ile90insLys
XM_011514556.1:c.301_302insAAA XP_011512858.1:p.Gln100_Ile101insLys
XM_011514557.1:c.268_269insAAA XP_011512859.1:p.Gln89_Ile90insLys
XR_926175.1:n.278_279insAAA
NM_005514.7:c.268_269insAAA NP_005505.2:p.Gln89_Ile90insLys
NM_005514.8:c.268_269insAAA MANE Select NP_005505.2:p.Gln89_Ile90insLys