Canonical Allele Identifier: CA2770463971

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29944657_29944658insGCTTTACAAAAGAGTAAGTGCTGG , CM000668.2:g.29944657_29944658insGCTTTACAAAAGAGTAAGTGCTGG	GRCh38
NC_000006.11:g.29912434_29912435insGCTTTACAAAAGAGTAAGTGCTGG , CM000668.1:g.29912434_29912435insGCTTTACAAAAGAGTAAGTGCTGG	GRCh37
NC_000006.10:g.30020413_30020414insGCTTTACAAAAGAGTAAGTGCTGG	NCBI36
NG_029217.2:g.7193_7194insGCTTTACAAAAGAGTAAGTGCTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.895+260_895+261insGCTTTACAAAAGAGTAAGTGCTGG	ENSP00000492789.2:n.895+260_895+261insGCTTTACAAAAGAGTAAGTGCTG...
ENST00000706892.1:n.2009_2010insGCTTTACAAAAGAGTAAGTGCTGG
ENST00000706893.1:c.1064+23_1064+24insGCTTTACAAAAGAGTAAGTGCTGG	ENSP00000516609.1:n.1064+23_1064+24insGCTTTACAAAAGAGTAAGTGCTG...
ENST00000706894.1:c.1012+41_1012+42insGCTTTACAAAAGAGTAAGTGCTGG	ENSP00000516610.1:n.1012+41_1012+42insGCTTTACAAAAGAGTAAGTGCTG...
ENST00000706895.1:n.1431_1432insGCTTTACAAAAGAGTAAGTGCTGG
ENST00000706896.1:n.1907_1908insGCTTTACAAAAGAGTAAGTGCTGG
ENST00000706897.1:n.1329_1330insGCTTTACAAAAGAGTAAGTGCTGG
ENST00000706898.1:c.1030+23_1030+24insGCTTTACAAAAGAGTAAGTGCTGG	ENSP00000516611.1:n.1030+23_1030+24insGCTTTACAAAAGAGTAAGTGCTG...
ENST00000706899.1:n.1866+41_1866+42insGCTTTACAAAAGAGTAAGTGCTGG
ENST00000706900.1:c.928+41_928+42insGCTTTACAAAAGAGTAAGTGCTGG	ENSP00000516617.1:n.928+41_928+42insGCTTTACAAAAGAGTAAGTGCTGG
ENST00000706901.1:c.1012+41_1012+42insGCTTTACAAAAGAGTAAGTGCTGG	ENSP00000516612.1:n.1012+41_1012+42insGCTTTACAAAAGAGTAAGTGCTG...
ENST00000706902.1:c.1012+41_1012+42insGCTTTACAAAAGAGTAAGTGCTGG	ENSP00000516613.1:n.1012+41_1012+42insGCTTTACAAAAGAGTAAGTGCTG...
ENST00000706903.1:c.1012+41_1012+42insGCTTTACAAAAGAGTAAGTGCTGG	ENSP00000516614.1:n.1012+41_1012+42insGCTTTACAAAAGAGTAAGTGCTG...
ENST00000706904.1:c.1012+41_1012+42insGCTTTACAAAAGAGTAAGTGCTGG	ENSP00000516615.1:n.1012+41_1012+42insGCTTTACAAAAGAGTAAGTGCTG...
ENST00000706905.1:c.1012+41_1012+42insGCTTTACAAAAGAGTAAGTGCTGG	ENSP00000516616.1:n.1012+41_1012+42insGCTTTACAAAAGAGTAAGTGCTG...
ENST00000376809.10:c.1012+41_1012+42insGCTTTACAAAAGAGTAAGTGCTGG MANE Select	ENSP00000366005.5:n.1012+41_1012+42insGCTTTACAAAAGAGTAAGTGCTG...
ENST00000638375.1:c.895+260_895+261insGCTTTACAAAAGAGTAAGTGCTGG	ENSP00000492789.1:n.895+260_895+261insGCTTTACAAAAGAGTAAGTGCTG...
ENST00000376802.2:c.895+260_895+261insGCTTTACAAAAGAGTAAGTGCTGG	ENSP00000365998.2:n.895+260_895+261insGCTTTACAAAAGAGTAAGTGCTG...
ENST00000376806.9:c.1030+23_1030+24insGCTTTACAAAAGAGTAAGTGCTGG	ENSP00000366002.5:n.1030+23_1030+24insGCTTTACAAAAGAGTAAGTGCTG...
ENST00000376809.9:c.1012+41_1012+42insGCTTTACAAAAGAGTAAGTGCTGG	ENSP00000366005.5:n.1012+41_1012+42insGCTTTACAAAAGAGTAAGTGCTG...
ENST00000396634.5:c.1012+41_1012+42insGCTTTACAAAAGAGTAAGTGCTGG	ENSP00000379873.1:n.1012+41_1012+42insGCTTTACAAAAGAGTAAGTGCTG...
ENST00000461903.1:n.1271+23_1271+24insGCTTTACAAAAGAGTAAGTGCTGG
ENST00000479320.5:n.1253+41_1253+42insGCTTTACAAAAGAGTAAGTGCTGG
ENST00000495183.5:n.1255+41_1255+42insGCTTTACAAAAGAGTAAGTGCTGG
ENST00000496081.5:n.870_871insGCTTTACAAAAGAGTAAGTGCTGG
NM_002116.7:c.1012+41_1012+42insGCTTTACAAAAGAGTAAGTGCTGG	NP_002107.3:n.1012+41_1012+42insGCTTTACAAAAGAGTAAGTGCTGG
NM_002116.8:c.1012+41_1012+42insGCTTTACAAAAGAGTAAGTGCTGG MANE Select	NP_002107.3:n.1012+41_1012+42insGCTTTACAAAAGAGTAAGTGCTGG