Canonical Allele Identifier: CA1619078661

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269988_31269997delinsCATAGCGGTG , CM000668.2:g.31269988_31269997delinsCATAGCGGTG	GRCh38
NC_000006.11:g.31237765_31237774delinsCATAGCGGTG , CM000668.1:g.31237765_31237774delinsCATAGCGGTG	GRCh37
NC_000006.10:g.31345744_31345753delinsCATAGCGGTG	NCBI36
NG_029422.2:g.7135_7144delinsCACCGCTATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.984_993delinsCACCGCTATG MANE Select	ENSP00000365402.5:p.Val328=
ENST00000376228.9:c.984_993delinsCACCGCTATG	ENSP00000365402.5:p.Val328=
ENST00000376237.8:c.*571_*580delinsCACCGCTATG	ENSP00000365412.4:n.*571_*580delinsCACCGCTATG
ENST00000383329.7:c.984_993delinsCACCGCTATG	ENSP00000372819.3:p.Val328=
ENST00000470363.5:n.302_311delinsCACCGCTATG
ENST00000487245.5:n.1343_1352delinsCACCGCTATG
NM_002117.5:c.984_993delinsCACCGCTATG	NP_002108.4:p.Val328=
NM_002117.6:c.984_993delinsCACCGCTATG MANE Select	NP_002108.4:p.Val328=