Canonical Allele Identifier: CA1619080090

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270690_31270691delinsCT , CM000668.2:g.31270690_31270691delinsCT	GRCh38
NC_000006.11:g.31238467_31238468delinsCT , CM000668.1:g.31238467_31238468delinsCT	GRCh37
NC_000006.10:g.31346446_31346447delinsCT	NCBI36
NG_029422.2:g.6441_6442delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.620-206_620-205delinsAG MANE Select	ENSP00000365402.5:n.620-206_620-205delinsAG
ENST00000376228.9:c.620-206_620-205delinsAG	ENSP00000365402.5:n.620-206_620-205delinsAG
ENST00000376237.8:c.*207-206_*207-205delinsAG	ENSP00000365412.4:n.*207-206_*207-205delinsAG
ENST00000383329.7:c.620-206_620-205delinsAG	ENSP00000372819.3:n.620-206_620-205delinsAG
ENST00000415537.1:c.618-206_618-205delinsAG
ENST00000487245.5:n.979-206_979-205delinsAG
ENST00000495835.1:n.809-206_809-205delinsAG
NM_002117.5:c.620-206_620-205delinsAG	NP_002108.4:n.620-206_620-205delinsAG
NM_002117.6:c.620-206_620-205delinsAG MANE Select	NP_002108.4:n.620-206_620-205delinsAG