Canonical Allele Identifier: CA449374707

Gene: HLA-A

Linked Data

• dbSNP Id: rs1770961753
• gnomAD v3: 6-29942661-G-A
• gnomAD v4: 6-29942661-G-A
• MyVariant Identifiers: chr6:g.29910438G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29942661G>A , CM000668.2:g.29942661G>A	GRCh38
NC_000006.11:g.29910438G>A , CM000668.1:g.29910438G>A	GRCh37
NC_000006.10:g.30018417G>A	NCBI36
NG_029217.2:g.5196G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000638375.2:c.73+35G>A	ENSP00000492789.2:n.73+35G>A
ENST00000706892.1:n.349+35G>A
ENST00000706893.1:c.73+35G>A	ENSP00000516609.1:n.73+35G>A
ENST00000706894.1:c.73+35G>A	ENSP00000516610.1:n.73+35G>A
ENST00000706895.1:n.349+35G>A
ENST00000706896.1:n.349+35G>A
ENST00000706897.1:n.349+35G>A
ENST00000706898.1:c.73+35G>A	ENSP00000516611.1:n.73+35G>A
ENST00000706899.1:n.349+35G>A
ENST00000706901.1:c.73+35G>A	ENSP00000516612.1:n.73+35G>A
ENST00000706902.1:c.73+35G>A	ENSP00000516613.1:n.73+35G>A
ENST00000706903.1:c.73+35G>A	ENSP00000516614.1:n.73+35G>A
ENST00000706904.1:c.73+35G>A	ENSP00000516615.1:n.73+35G>A
ENST00000706905.1:c.73+35G>A	ENSP00000516616.1:n.73+35G>A
ENST00000376809.10:c.73+35G>A MANE Select	ENSP00000366005.5:n.73+35G>A
ENST00000638375.1:c.73+35G>A	ENSP00000492789.1:n.73+35G>A
ENST00000376802.2:c.73+35G>A	ENSP00000365998.2:n.73+35G>A
ENST00000376806.9:c.73+35G>A	ENSP00000366002.5:n.73+35G>A
ENST00000376809.9:c.73+35G>A	ENSP00000366005.5:n.73+35G>A
ENST00000396634.5:c.73+35G>A	ENSP00000379873.1:n.73+35G>A
ENST00000429656.1:n.407C>T
ENST00000461903.1:n.73+35G>A
ENST00000479320.5:n.73+35G>A
ENST00000495183.5:n.75+35G>A
ENST00000496081.5:n.79+35G>A
NM_002116.7:c.73+35G>A	NP_002107.3:n.73+35G>A
NM_002116.8:c.73+35G>A MANE Select	NP_002107.3:n.73+35G>A