Canonical Allele Identifier: CA3693162

Gene: HLA-A

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29942975G>C , CM000668.2:g.29942975G>C	GRCh38
NC_000006.11:g.29910752G>C , CM000668.1:g.29910752G>C	GRCh37
NC_000006.10:g.30018731G>C	NCBI36
NG_029217.2:g.5510G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.292G>C	ENSP00000492789.2:p.Asp98His
ENST00000706892.1:n.568G>C
ENST00000706893.1:c.292G>C	ENSP00000516609.1:p.Asp98His
ENST00000706894.1:c.292G>C	ENSP00000516610.1:p.Asp98His
ENST00000706895.1:n.568G>C
ENST00000706896.1:n.568G>C
ENST00000706897.1:n.568G>C
ENST00000706898.1:c.292G>C	ENSP00000516611.1:p.Asp98His
ENST00000706899.1:n.568G>C
ENST00000706900.1:c.208G>C	ENSP00000516617.1:p.Asp70His
ENST00000706901.1:c.292G>C	ENSP00000516612.1:p.Asp98His
ENST00000706902.1:c.292G>C	ENSP00000516613.1:p.Asp98His
ENST00000706903.1:c.292G>C	ENSP00000516614.1:p.Asp98His
ENST00000706904.1:c.292G>C	ENSP00000516615.1:p.Asp98His
ENST00000706905.1:c.292G>C	ENSP00000516616.1:p.Asp98His
ENST00000376809.10:c.292G>C MANE Select	ENSP00000366005.5:p.Asp98His
ENST00000638375.1:c.292G>C	ENSP00000492789.1:p.Asp98His
ENST00000376802.2:c.292G>C	ENSP00000365998.2:p.Asp98His
ENST00000376806.9:c.292G>C	ENSP00000366002.5:p.Asp98His
ENST00000376809.9:c.292G>C	ENSP00000366005.5:p.Asp98His
ENST00000396634.5:c.292G>C	ENSP00000379873.1:p.Asp98His
ENST00000429656.1:n.93C>G
ENST00000461903.1:n.292G>C
ENST00000479320.5:n.292G>C
ENST00000495183.5:n.294G>C
ENST00000496081.5:n.177+121G>C
NM_002116.7:c.292G>C	NP_002107.3:p.Asp98His
NM_002116.8:c.292G>C MANE Select	NP_002107.3:p.Asp98His