Canonical Allele Identifier: CA1619113023

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356757_31356758delinsTG , CM000668.2:g.31356757_31356758delinsTG	GRCh38
NC_000006.11:g.31324534_31324535delinsTG , CM000668.1:g.31324534_31324535delinsTG	GRCh37
NC_000006.10:g.31432513_31432514delinsTG	NCBI36
NG_023187.1:g.5455_5456delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1746_1747delinsCA
ENST00000481849.6:n.1746_1747delinsCA
ENST00000497377.6:n.1746_1747delinsCA
ENST00000640094.2:c.273_274delinsCA	ENSP00000491275.2:p.Tyr91=
ENST00000696558.1:c.273_274delinsCA	ENSP00000512716.1:p.Tyr91=
ENST00000696559.1:c.273_274delinsCA	ENSP00000512717.1:p.Tyr91=
ENST00000696560.1:c.273_274delinsCA	ENSP00000512718.1:p.Tyr91=
ENST00000696561.1:c.273_274delinsCA	ENSP00000512719.1:p.Tyr91=
ENST00000696562.1:c.273_274delinsCA	ENSP00000512720.1:p.Tyr91=
ENST00000412585.7:c.273_274delinsCA MANE Select	ENSP00000399168.2:p.Tyr91=
ENST00000412585.6:c.273_274delinsCA	ENSP00000399168.2:p.Tyr91=
ENST00000434333.1:c.306_307delinsCA	ENSP00000405931.1:p.Tyr102=
ENST00000474381.1:n.148_149delinsCA
ENST00000498007.1:n.294_295delinsCA
ENST00000603274.1:n.111_112delinsTG
NM_005514.6:c.273_274delinsCA	NP_005505.2:p.Tyr91=
XM_011514556.1:c.306_307delinsCA	XP_011512858.1:p.Tyr102=
XM_011514557.1:c.273_274delinsCA	XP_011512859.1:p.Tyr91=
XR_926175.1:n.283_284delinsCA
NM_005514.7:c.273_274delinsCA	NP_005505.2:p.Tyr91=
NM_005514.8:c.273_274delinsCA MANE Select	NP_005505.2:p.Tyr91=