Canonical Allele Identifier: CA2677796561

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29945245-GCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945247_29945248del , CM000668.2:g.29945247_29945248del	GRCh38
NC_000006.11:g.29913024_29913025del , CM000668.1:g.29913024_29913025del	GRCh37
NC_000006.10:g.30021003_30021004del	NCBI36
NG_029217.2:g.7783_7784del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.942_943del	ENSP00000492789.2:p.Gln315GlyfsTer3
ENST00000706892.1:n.2599_2600del
ENST00000706893.1:c.*43_*44del	ENSP00000516609.1:n.*43_*44del
ENST00000706894.1:c.1059_1060del	ENSP00000516610.1:p.Gln354GlyfsTer3
ENST00000706895.1:n.1879_1880del
ENST00000706896.1:n.2355_2356del
ENST00000706897.1:n.1777_1778del
ENST00000706898.1:c.1077_1078del	ENSP00000516611.1:p.Gln360GlyfsTer3
ENST00000706899.1:n.1913_1914del
ENST00000706900.1:c.975_976del	ENSP00000516617.1:p.Gln326GlyfsTer3
ENST00000706901.1:c.1059_1060del	ENSP00000516612.1:p.Gln354GlyfsTer3
ENST00000706902.1:c.1059_1060del	ENSP00000516613.1:p.Gln354GlyfsTer3
ENST00000706903.1:c.1059_1060del	ENSP00000516614.1:p.Gln354GlyfsTer3
ENST00000706904.1:c.1059_1060del	ENSP00000516615.1:p.Gln354GlyfsTer3
ENST00000706905.1:c.1059_1060del	ENSP00000516616.1:p.Gln354GlyfsTer3
ENST00000376809.10:c.1059_1060del MANE Select	ENSP00000366005.5:p.Gln354GlyfsTer3
ENST00000638375.1:c.942_943del	ENSP00000492789.1:p.Gln315GlyfsTer3
ENST00000376802.2:c.896-204_896-203del	ENSP00000365998.2:n.896-204_896-203del
ENST00000376806.9:c.1077_1078del	ENSP00000366002.5:p.Gln360GlyfsTer3
ENST00000376809.9:c.1059_1060del	ENSP00000366005.5:p.Gln354GlyfsTer3
ENST00000396634.5:c.1059_1060del	ENSP00000379873.1:p.Gln354GlyfsTer3
ENST00000461903.1:n.1318_1319del
ENST00000479320.5:n.1300_1301del
ENST00000495183.5:n.1298_1299del
ENST00000496081.5:n.1318_1319del
NM_002116.7:c.1059_1060del	NP_002107.3:p.Gln354GlyfsTer3
NM_002116.8:c.1059_1060del MANE Select	NP_002107.3:p.Gln354GlyfsTer3