Canonical Allele Identifier: CA1619118276

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355159_31355165delinsAACTGCT , CM000668.2:g.31355159_31355165delinsAACTGCT	GRCh38
NC_000006.11:g.31322936_31322942delinsAACTGCT , CM000668.1:g.31322936_31322942delinsAACTGCT	GRCh37
NC_000006.10:g.31430915_31430921delinsAACTGCT	NCBI36
NG_023187.1:g.7048_7054delinsAGCAGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3001_3007delinsAGCAGTT
ENST00000481849.6:n.2520_2526delinsAGCAGTT
ENST00000497377.6:n.2427_2433delinsAGCAGTT
ENST00000640094.2:c.895+152_895+158delinsAGCAGTT	ENSP00000491275.2:n.895+152_895+158delinsAGCAGTT
ENST00000696558.1:c.1023_1029delinsAGCAGTT	ENSP00000512716.1:n.1023_1029delinsAGCAGTT
ENST00000696559.1:c.954_960delinsAGCAGTT	ENSP00000512717.1:p.Leu318=
ENST00000696560.1:c.954_960delinsAGCAGTT	ENSP00000512718.1:p.Leu318=
ENST00000696561.1:c.954_960delinsAGCAGTT	ENSP00000512719.1:p.Leu318=
ENST00000696562.1:c.954_960delinsAGCAGTT	ENSP00000512720.1:p.Leu318=
ENST00000412585.7:c.954_960delinsAGCAGTT MANE Select	ENSP00000399168.2:p.Leu318=
ENST00000640094.1:c.88+152_88+158delinsAGCAGTT	ENSP00000491275.1:n.88+152_88+158delinsAGCAGTT
ENST00000412585.6:c.954_960delinsAGCAGTT	ENSP00000399168.2:p.Leu318=
ENST00000463574.1:n.545_551delinsAGCAGTT
NM_005514.6:c.954_960delinsAGCAGTT	NP_005505.2:p.Leu318=
XM_011514556.1:c.987_993delinsAGCAGTT	XP_011512858.1:p.Leu329=
XM_011514557.1:c.895+152_895+158delinsAGCAGTT	XP_011512859.1:n.895+152_895+158delinsAGCAGTT
XR_926175.1:n.1393_1399delinsAGCAGTT
NM_005514.7:c.954_960delinsAGCAGTT	NP_005505.2:p.Leu318=
NM_005514.8:c.954_960delinsAGCAGTT MANE Select	NP_005505.2:p.Leu318=