Canonical Allele Identifier: CA650786148

Gene: HLA-B

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357161_31357162insT , CM000668.2:g.31357161_31357162insT	GRCh38
NC_000006.11:g.31324938_31324939insT , CM000668.1:g.31324938_31324939insT	GRCh37
NC_000006.10:g.31432917_31432918insT	NCBI36
NG_023187.1:g.5051_5052insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1470_1471insA
ENST00000481849.6:n.1470_1471insA
ENST00000497377.6:n.1470_1471insA
ENST00000696559.1:c.-4_-3insA	ENSP00000512717.1:n.-4_-3insA
ENST00000696560.1:c.-4_-3insA	ENSP00000512718.1:n.-4_-3insA
ENST00000696561.1:c.-4_-3insA	ENSP00000512719.1:n.-4_-3insA
ENST00000696562.1:c.-4_-3insA	ENSP00000512720.1:n.-4_-3insA
ENST00000412585.7:c.-4_-3insA MANE Select	ENSP00000399168.2:n.-4_-3insA
ENST00000412585.6:c.-4_-3insA	ENSP00000399168.2:n.-4_-3insA
ENST00000434333.1:c.-99_-98insA	ENSP00000405931.1:n.-99_-98insA
ENST00000498007.1:n.18_19insA
ENST00000603274.1:n.515_516insT
NM_005514.6:c.-4_-3insA	NP_005505.2:n.-4_-3insA
XM_011514557.1:c.-4_-3insA	XP_011512859.1:n.-4_-3insA
XR_926175.1:n.7_8insA
NM_005514.7:c.-4_-3insA	NP_005505.2:n.-4_-3insA
NM_005514.8:c.-4_-3insA MANE Select	NP_005505.2:n.-4_-3insA