Canonical Allele Identifier: CA449461033

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29942797-G-C
• MyVariant Identifiers: chr6:g.29910574G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29942797G>C , CM000668.2:g.29942797G>C	GRCh38
NC_000006.11:g.29910574G>C , CM000668.1:g.29910574G>C	GRCh37
NC_000006.10:g.30018553G>C	NCBI36
NG_029217.2:g.5332G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000638375.2:c.114G>C	ENSP00000492789.2:p.Arg38=
ENST00000706892.1:n.390G>C
ENST00000706893.1:c.114G>C	ENSP00000516609.1:p.Arg38=
ENST00000706894.1:c.114G>C	ENSP00000516610.1:p.Arg38=
ENST00000706895.1:n.390G>C
ENST00000706896.1:n.390G>C
ENST00000706897.1:n.390G>C
ENST00000706898.1:c.114G>C	ENSP00000516611.1:p.Arg38=
ENST00000706899.1:n.390G>C
ENST00000706900.1:c.30G>C	ENSP00000516617.1:p.Arg10=
ENST00000706901.1:c.114G>C	ENSP00000516612.1:p.Arg38=
ENST00000706902.1:c.114G>C	ENSP00000516613.1:p.Arg38=
ENST00000706903.1:c.114G>C	ENSP00000516614.1:p.Arg38=
ENST00000706904.1:c.114G>C	ENSP00000516615.1:p.Arg38=
ENST00000706905.1:c.114G>C	ENSP00000516616.1:p.Arg38=
ENST00000376809.10:c.114G>C MANE Select	ENSP00000366005.5:p.Arg38=
ENST00000638375.1:c.114G>C	ENSP00000492789.1:p.Arg38=
ENST00000376802.2:c.114G>C	ENSP00000365998.2:p.Arg38=
ENST00000376806.9:c.114G>C	ENSP00000366002.5:p.Arg38=
ENST00000376809.9:c.114G>C	ENSP00000366005.5:p.Arg38=
ENST00000396634.5:c.114G>C	ENSP00000379873.1:p.Arg38=
ENST00000429656.1:n.271C>G
ENST00000461903.1:n.114G>C
ENST00000479320.5:n.114G>C
ENST00000495183.5:n.116G>C
ENST00000496081.5:n.120G>C
NM_002116.7:c.114G>C	NP_002107.3:p.Arg38=
NM_002116.8:c.114G>C MANE Select	NP_002107.3:p.Arg38=