Canonical Allele Identifier: CA2770463953
Gene: HLA-A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29944123_29944124insT , CM000668.2:g.29944123_29944124insT GRCh38
NC_000006.11:g.29911900_29911901insT , CM000668.1:g.29911900_29911901insT GRCh37
NC_000006.10:g.30019879_30019880insT NCBI36
NG_029217.2:g.6659_6660insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.621_622insT ENSP00000492789.2:p.Pro208SerfsTer13
ENST00000706892.1:n.1475_1476insT
ENST00000706893.1:c.621_622insT ENSP00000516609.1:p.Pro208SerfsTer13
ENST00000706894.1:c.621_622insT ENSP00000516610.1:p.Pro208SerfsTer13
ENST00000706895.1:n.897_898insT
ENST00000706896.1:n.1475_1476insT
ENST00000706897.1:n.897_898insT
ENST00000706898.1:c.621_622insT ENSP00000516611.1:p.Pro208SerfsTer13
ENST00000706899.1:n.1475_1476insT
ENST00000706900.1:c.537_538insT ENSP00000516617.1:p.Pro180SerfsTer13
ENST00000706901.1:c.621_622insT ENSP00000516612.1:p.Pro208SerfsTer13
ENST00000706902.1:c.621_622insT ENSP00000516613.1:p.Pro208SerfsTer13
ENST00000706903.1:c.621_622insT ENSP00000516614.1:p.Pro208SerfsTer13
ENST00000706904.1:c.621_622insT ENSP00000516615.1:p.Pro208SerfsTer13
ENST00000706905.1:c.621_622insT ENSP00000516616.1:p.Pro208SerfsTer13
ENST00000376809.10:c.621_622insT MANE Select ENSP00000366005.5:p.Pro208SerfsTer13
ENST00000638375.1:c.621_622insT ENSP00000492789.1:p.Pro208SerfsTer13
ENST00000376802.2:c.621_622insT ENSP00000365998.2:p.Pro208SerfsTer13
ENST00000376806.9:c.621_622insT ENSP00000366002.5:p.Pro208SerfsTer13
ENST00000376809.9:c.621_622insT ENSP00000366005.5:p.Pro208SerfsTer13
ENST00000396634.5:c.621_622insT ENSP00000379873.1:p.Pro208SerfsTer13
ENST00000461903.1:n.862_863insT
ENST00000479320.5:n.862_863insT
ENST00000495183.5:n.864_865insT
ENST00000496081.5:n.438_439insT
NM_002116.7:c.621_622insT NP_002107.3:p.Pro208SerfsTer13
NM_002116.8:c.621_622insT MANE Select NP_002107.3:p.Pro208SerfsTer13