Canonical Allele Identifier: CA3693666

Gene: HLA-A

Linked Data

• dbSNP Id: rs777825089
• ExAC: 6:29912414 G / GAAGGGT
• MyVariant Identifiers: chr6:g.29912414_29912415insAAGGGT (hg19) ; chr6:g.29944637_29944638insAAGGGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29944637_29944638insAAGGGT , CM000668.2:g.29944637_29944638insAAGGGT	GRCh38
NC_000006.11:g.29912414_29912415insAAGGGT , CM000668.1:g.29912414_29912415insAAGGGT	GRCh37
NC_000006.10:g.30020393_30020394insAAGGGT	NCBI36
NG_029217.2:g.7173_7174insAAGGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.895+240_895+241insAAGGGT	ENSP00000492789.2:n.895+240_895+241insAAGGGT
ENST00000706892.1:n.1989_1990insAAGGGT
ENST00000706893.1:c.1064+3_1064+4insAAGGGT	ENSP00000516609.1:n.1064+3_1064+4insAAGGGT
ENST00000706894.1:c.1012+21_1012+22insAAGGGT	ENSP00000516610.1:n.1012+21_1012+22insAAGGGT
ENST00000706895.1:n.1411_1412insAAGGGT
ENST00000706896.1:n.1887_1888insAAGGGT
ENST00000706897.1:n.1309_1310insAAGGGT
ENST00000706898.1:c.1030+3_1030+4insAAGGGT	ENSP00000516611.1:n.1030+3_1030+4insAAGGGT
ENST00000706899.1:n.1866+21_1866+22insAAGGGT
ENST00000706900.1:c.928+21_928+22insAAGGGT	ENSP00000516617.1:n.928+21_928+22insAAGGGT
ENST00000706901.1:c.1012+21_1012+22insAAGGGT	ENSP00000516612.1:n.1012+21_1012+22insAAGGGT
ENST00000706902.1:c.1012+21_1012+22insAAGGGT	ENSP00000516613.1:n.1012+21_1012+22insAAGGGT
ENST00000706903.1:c.1012+21_1012+22insAAGGGT	ENSP00000516614.1:n.1012+21_1012+22insAAGGGT
ENST00000706904.1:c.1012+21_1012+22insAAGGGT	ENSP00000516615.1:n.1012+21_1012+22insAAGGGT
ENST00000706905.1:c.1012+21_1012+22insAAGGGT	ENSP00000516616.1:n.1012+21_1012+22insAAGGGT
ENST00000376809.10:c.1012+21_1012+22insAAGGGT MANE Select	ENSP00000366005.5:n.1012+21_1012+22insAAGGGT
ENST00000638375.1:c.895+240_895+241insAAGGGT	ENSP00000492789.1:n.895+240_895+241insAAGGGT
ENST00000376802.2:c.895+240_895+241insAAGGGT	ENSP00000365998.2:n.895+240_895+241insAAGGGT
ENST00000376806.9:c.1030+3_1030+4insAAGGGT	ENSP00000366002.5:n.1030+3_1030+4insAAGGGT
ENST00000376809.9:c.1012+21_1012+22insAAGGGT	ENSP00000366005.5:n.1012+21_1012+22insAAGGGT
ENST00000396634.5:c.1012+21_1012+22insAAGGGT	ENSP00000379873.1:n.1012+21_1012+22insAAGGGT
ENST00000461903.1:n.1271+3_1271+4insAAGGGT
ENST00000479320.5:n.1253+21_1253+22insAAGGGT
ENST00000495183.5:n.1255+21_1255+22insAAGGGT
ENST00000496081.5:n.850_851insAAGGGT
NM_002116.7:c.1012+21_1012+22insAAGGGT	NP_002107.3:n.1012+21_1012+22insAAGGGT
NM_002116.8:c.1012+21_1012+22insAAGGGT MANE Select	NP_002107.3:n.1012+21_1012+22insAAGGGT