Canonical Allele Identifier: CA2677955003

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355141-C-CATAGCTCCTAGG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355142_31355143insTAGCTCCTAGGA , CM000668.2:g.31355142_31355143insTAGCTCCTAGGA	GRCh38
NC_000006.11:g.31322919_31322920insTAGCTCCTAGGA , CM000668.1:g.31322919_31322920insTAGCTCCTAGGA	GRCh37
NC_000006.10:g.31430898_31430899insTAGCTCCTAGGA	NCBI36
NG_023187.1:g.7071_7072insCCTAGGAGCTAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3024_3025insCCTAGGAGCTAT
ENST00000481849.6:n.2543_2544insCCTAGGAGCTAT
ENST00000497377.6:n.2450_2451insCCTAGGAGCTAT
ENST00000640094.2:c.895+175_895+176insCCTAGGAGCTAT	ENSP00000491275.2:n.895+175_895+176insCCT...
ENST00000696558.1:c.1046_1047insCCTAGGAGCTAT	ENSP00000512716.1:n.1046_1047insCCTAGGAGC...
ENST00000696559.1:c.977_978insCCTAGGAGCTAT	ENSP00000512717.1:p.Val326_Val327insLeuGl...
ENST00000696560.1:c.977_978insCCTAGGAGCTAT	ENSP00000512718.1:p.Val326_Val327insLeuGl...
ENST00000696561.1:c.977_978insCCTAGGAGCTAT	ENSP00000512719.1:p.Val326_Val327insLeuGl...
ENST00000696562.1:c.977_978insCCTAGGAGCTAT	ENSP00000512720.1:p.Val326_Val327insLeuGl...
ENST00000412585.7:c.977_978insCCTAGGAGCTAT MANE Select	ENSP00000399168.2:p.Val326_Val327insLeuGl...
ENST00000640094.1:c.88+175_88+176insCCTAGGAGCTAT	ENSP00000491275.1:n.88+175_88+176insCCTAG...
ENST00000412585.6:c.977_978insCCTAGGAGCTAT	ENSP00000399168.2:p.Val326_Val327insLeuGl...
ENST00000463574.1:n.568_569insCCTAGGAGCTAT
NM_005514.6:c.977_978insCCTAGGAGCTAT	NP_005505.2:p.Val326_Val327insLeuGlyAlaMe...
XM_011514556.1:c.1010_1011insCCTAGGAGCTAT	XP_011512858.1:p.Val337_Val338insLeuGlyAl...
XM_011514557.1:c.895+175_895+176insCCTAGGAGCTAT	XP_011512859.1:n.895+175_895+176insCCTAGG...
XR_926175.1:n.1416_1417insCCTAGGAGCTAT
NM_005514.7:c.977_978insCCTAGGAGCTAT	NP_005505.2:p.Val326_Val327insLeuGlyAlaMe...
NM_005514.8:c.977_978insCCTAGGAGCTAT MANE Select	NP_005505.2:p.Val326_Val327insLeuGlyAlaMe...