Canonical Allele Identifier: CA2770491443

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270760_31270761insCAGGCAGAGAACAAGGCCT , CM000668.2:g.31270760_31270761insCAGGCAGAGAACAAGGCCT	GRCh38
NC_000006.11:g.31238537_31238538insCAGGCAGAGAACAAGGCCT , CM000668.1:g.31238537_31238538insCAGGCAGAGAACAAGGCCT	GRCh37
NC_000006.10:g.31346516_31346517insCAGGCAGAGAACAAGGCCT	NCBI36
NG_029422.2:g.6372_6373insGGCCTTGTTCTCTGCCTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.620-275_620-274insGGCCTTGTTCTCTGCCTGA MANE Select	ENSP00000365402.5:n.620-275_620-274insGGCCTTGTTCTCTGCCTGA
ENST00000376228.9:c.620-275_620-274insGGCCTTGTTCTCTGCCTGA	ENSP00000365402.5:n.620-275_620-274insGGCCTTGTTCTCTGCCTGA
ENST00000376237.8:c.*207-275_*207-274insGGCCTTGTTCTCTGCCTGA	ENSP00000365412.4:n.*207-275_*207-274insGGCCTTGTTCTCTGCCTGA
ENST00000383329.7:c.620-275_620-274insGGCCTTGTTCTCTGCCTGA	ENSP00000372819.3:n.620-275_620-274insGGCCTTGTTCTCTGCCTGA
ENST00000415537.1:c.618-275_618-274insGGCCTTGTTCTCTGCCTGA
ENST00000487245.5:n.979-275_979-274insGGCCTTGTTCTCTGCCTGA
ENST00000495835.1:n.809-275_809-274insGGCCTTGTTCTCTGCCTGA
NM_002117.5:c.620-275_620-274insGGCCTTGTTCTCTGCCTGA	NP_002108.4:n.620-275_620-274insGGCCTTGTTCTCTGCCTGA
NM_002117.6:c.620-275_620-274insGGCCTTGTTCTCTGCCTGA MANE Select	NP_002108.4:n.620-275_620-274insGGCCTTGTTCTCTGCCTGA