Canonical Allele Identifier: CA2832547558

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270150_31270151del , CM000668.2:g.31270150_31270151del	GRCh38
NC_000006.11:g.31237927_31237928del , CM000668.1:g.31237927_31237928del	GRCh37
NC_000006.10:g.31345906_31345907del	NCBI36
NG_029422.2:g.6981_6982del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.895+59_895+60del MANE Select	ENSP00000365402.5:n.895+59_895+60del
ENST00000376228.9:c.895+59_895+60del	ENSP00000365402.5:n.895+59_895+60del
ENST00000376237.8:c.*482+59_*482+60del	ENSP00000365412.4:n.*482+59_*482+60del
ENST00000383329.7:c.895+59_895+60del	ENSP00000372819.3:n.895+59_895+60del
ENST00000470363.5:n.213+59_213+60del
ENST00000487245.5:n.1254+59_1254+60del
NM_002117.5:c.895+59_895+60del	NP_002108.4:n.895+59_895+60del
NM_002117.6:c.895+59_895+60del MANE Select	NP_002108.4:n.895+59_895+60del