Canonical Allele Identifier: CA1619118039

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355064_31355065delinsTG , CM000668.2:g.31355064_31355065delinsTG	GRCh38
NC_000006.11:g.31322841_31322842delinsTG , CM000668.1:g.31322841_31322842delinsTG	GRCh37
NC_000006.10:g.31430820_31430821delinsTG	NCBI36
NG_023187.1:g.7148_7149delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3059+42_3059+43delinsCA
ENST00000481849.6:n.2620_2621delinsCA
ENST00000497377.6:n.2527_2528delinsCA
ENST00000640094.2:c.895+252_895+253delinsCA	ENSP00000491275.2:n.895+252_895+253delinsCA
ENST00000696558.1:c.1081+42_1081+43delinsCA	ENSP00000512716.1:n.1081+42_1081+43delinsCA
ENST00000696559.1:c.1012+42_1012+43delinsCA	ENSP00000512717.1:n.1012+42_1012+43delinsCA
ENST00000696560.1:c.1012+42_1012+43delinsCA	ENSP00000512718.1:n.1012+42_1012+43delinsCA
ENST00000696561.1:c.1012+42_1012+43delinsCA	ENSP00000512719.1:n.1012+42_1012+43delinsCA
ENST00000696562.1:c.1012+42_1012+43delinsCA	ENSP00000512720.1:n.1012+42_1012+43delinsCA
ENST00000412585.7:c.1012+42_1012+43delinsCA MANE Select	ENSP00000399168.2:n.1012+42_1012+43delinsCA
ENST00000640094.1:c.88+252_88+253delinsCA	ENSP00000491275.1:n.88+252_88+253delinsCA
ENST00000412585.6:c.1012+42_1012+43delinsCA	ENSP00000399168.2:n.1012+42_1012+43delinsCA
ENST00000497377.5:n.12_13delinsCA
NM_005514.6:c.1012+42_1012+43delinsCA	NP_005505.2:n.1012+42_1012+43delinsCA
XM_011514556.1:c.1045+42_1045+43delinsCA	XP_011512858.1:n.1045+42_1045+43delinsCA
XM_011514557.1:c.895+252_895+253delinsCA	XP_011512859.1:n.895+252_895+253delinsCA
XR_926175.1:n.1451+42_1451+43delinsCA
NM_005514.7:c.1012+42_1012+43delinsCA	NP_005505.2:n.1012+42_1012+43delinsCA
NM_005514.8:c.1012+42_1012+43delinsCA MANE Select	NP_005505.2:n.1012+42_1012+43delinsCA