Canonical Allele Identifier: CA136836628

Gene: HLA-B

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356864_31356866delinsAGC , CM000668.2:g.31356864_31356866delinsAGC	GRCh38
NC_000006.11:g.31324641_31324643delinsAGC , CM000668.1:g.31324641_31324643delinsAGC	GRCh37
NC_000006.10:g.31432620_31432622delinsAGC	NCBI36
NG_023187.1:g.5347_5349delinsGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1638_1640delinsGCT
ENST00000481849.6:n.1638_1640delinsGCT
ENST00000497377.6:n.1638_1640delinsGCT
ENST00000640094.2:c.165_167delinsGCT	ENSP00000491275.2:p.Gln56Leu
ENST00000696558.1:c.165_167delinsGCT	ENSP00000512716.1:p.Gln56Leu
ENST00000696559.1:c.165_167delinsGCT	ENSP00000512717.1:p.Gln56Leu
ENST00000696560.1:c.165_167delinsGCT	ENSP00000512718.1:p.Gln56Leu
ENST00000696561.1:c.165_167delinsGCT	ENSP00000512719.1:p.Gln56Leu
ENST00000696562.1:c.165_167delinsGCT	ENSP00000512720.1:p.Gln56Leu
ENST00000412585.7:c.165_167delinsGCT MANE Select	ENSP00000399168.2:p.Gln56Leu
ENST00000412585.6:c.165_167delinsGCT	ENSP00000399168.2:p.Gln56Leu
ENST00000434333.1:c.198_200delinsGCT	ENSP00000405931.1:p.Gln67Leu
ENST00000474381.1:n.40_42delinsGCT
ENST00000498007.1:n.186_188delinsGCT
ENST00000603274.1:n.218_220delinsAGC
NM_005514.6:c.165_167delinsGCT	NP_005505.2:p.Gln56Leu
XM_011514556.1:c.198_200delinsGCT	XP_011512858.1:p.Gln67Leu
XM_011514557.1:c.165_167delinsGCT	XP_011512859.1:p.Gln56Leu
XR_926175.1:n.175_177delinsGCT
NM_005514.7:c.165_167delinsGCT	NP_005505.2:p.Gln56Leu
NM_005514.8:c.165_167delinsGCT MANE Select	NP_005505.2:p.Gln56Leu