Canonical Allele Identifier: CA2523403192

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356422_31356423insCA , CM000668.2:g.31356422_31356423insCA	GRCh38
NC_000006.11:g.31324199_31324200insCA , CM000668.1:g.31324199_31324200insCA	GRCh37
NC_000006.10:g.31432178_31432179insCA	NCBI36
NG_023187.1:g.5790_5791insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1836_1837insTG
ENST00000481849.6:n.1836_1837insTG
ENST00000497377.6:n.1836_1837insTG
ENST00000640094.2:c.363_364insTG	ENSP00000491275.2:p.Met122Ter
ENST00000696558.1:c.363_364insTG	ENSP00000512716.1:p.Met122Ter
ENST00000696559.1:c.363_364insTG	ENSP00000512717.1:p.Met122Ter
ENST00000696560.1:c.363_364insTG	ENSP00000512718.1:p.Met122Ter
ENST00000696561.1:c.363_364insTG	ENSP00000512719.1:p.Met122Ter
ENST00000696562.1:c.363_364insTG	ENSP00000512720.1:p.Met122Ter
ENST00000412585.7:c.363_364insTG MANE Select	ENSP00000399168.2:p.Met122Ter
ENST00000412585.6:c.363_364insTG	ENSP00000399168.2:p.Met122Ter
ENST00000434333.1:c.396_397insTG	ENSP00000405931.1:p.Met133Ter
ENST00000474381.1:n.238_239insTG
ENST00000498007.1:n.629_630insTG
NM_005514.6:c.363_364insTG	NP_005505.2:p.Met122Ter
XM_011514556.1:c.396_397insTG	XP_011512858.1:p.Met133Ter
XM_011514557.1:c.363_364insTG	XP_011512859.1:p.Met122Ter
XR_926175.1:n.373_374insTG
NM_005514.7:c.363_364insTG	NP_005505.2:p.Met122Ter
NM_005514.8:c.363_364insTG MANE Select	NP_005505.2:p.Met122Ter