Canonical Allele Identifier: CA3693663

Gene: HLA-A

Linked Data

• dbSNP Id: rs747654166
• ExAC: 6:29912412 G / GA
• MyVariant Identifiers: chr6:g.29912412_29912413insA (hg19) ; chr6:g.29944635_29944636insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29944635_29944636insA , CM000668.2:g.29944635_29944636insA	GRCh38
NC_000006.11:g.29912412_29912413insA , CM000668.1:g.29912412_29912413insA	GRCh37
NC_000006.10:g.30020391_30020392insA	NCBI36
NG_029217.2:g.7171_7172insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.895+238_895+239insA	ENSP00000492789.2:n.895+238_895+239insA
ENST00000706892.1:n.1987_1988insA
ENST00000706893.1:c.1064+1_1064+2insA	ENSP00000516609.1:n.1064+1_1064+2insA
ENST00000706894.1:c.1012+19_1012+20insA	ENSP00000516610.1:n.1012+19_1012+20insA
ENST00000706895.1:n.1409_1410insA
ENST00000706896.1:n.1885_1886insA
ENST00000706897.1:n.1307_1308insA
ENST00000706898.1:c.1030+1_1030+2insA	ENSP00000516611.1:n.1030+1_1030+2insA
ENST00000706899.1:n.1866+19_1866+20insA
ENST00000706900.1:c.928+19_928+20insA	ENSP00000516617.1:n.928+19_928+20insA
ENST00000706901.1:c.1012+19_1012+20insA	ENSP00000516612.1:n.1012+19_1012+20insA
ENST00000706902.1:c.1012+19_1012+20insA	ENSP00000516613.1:n.1012+19_1012+20insA
ENST00000706903.1:c.1012+19_1012+20insA	ENSP00000516614.1:n.1012+19_1012+20insA
ENST00000706904.1:c.1012+19_1012+20insA	ENSP00000516615.1:n.1012+19_1012+20insA
ENST00000706905.1:c.1012+19_1012+20insA	ENSP00000516616.1:n.1012+19_1012+20insA
ENST00000376809.10:c.1012+19_1012+20insA MANE Select	ENSP00000366005.5:n.1012+19_1012+20insA
ENST00000638375.1:c.895+238_895+239insA	ENSP00000492789.1:n.895+238_895+239insA
ENST00000376802.2:c.895+238_895+239insA	ENSP00000365998.2:n.895+238_895+239insA
ENST00000376806.9:c.1030+1_1030+2insA	ENSP00000366002.5:n.1030+1_1030+2insA
ENST00000376809.9:c.1012+19_1012+20insA	ENSP00000366005.5:n.1012+19_1012+20insA
ENST00000396634.5:c.1012+19_1012+20insA	ENSP00000379873.1:n.1012+19_1012+20insA
ENST00000461903.1:n.1271+1_1271+2insA
ENST00000479320.5:n.1253+19_1253+20insA
ENST00000495183.5:n.1255+19_1255+20insA
ENST00000496081.5:n.848_849insA
NM_002116.7:c.1012+19_1012+20insA	NP_002107.3:n.1012+19_1012+20insA
NM_002116.8:c.1012+19_1012+20insA MANE Select	NP_002107.3:n.1012+19_1012+20insA