Canonical Allele Identifier: CA3710349

Gene: HLA-C

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269987_31269988insAACAA , CM000668.2:g.31269987_31269988insAACAA	GRCh38
NC_000006.11:g.31237764_31237765insAACAA , CM000668.1:g.31237764_31237765insAACAA	GRCh37
NC_000006.10:g.31345743_31345744insAACAA	NCBI36
NG_029422.2:g.7144_7145insTTGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.993_994insTTGTT MANE Select	ENSP00000365402.5:p.Met332LeufsTer?
ENST00000376228.9:c.993_994insTTGTT	ENSP00000365402.5:p.Met332LeufsTer?
ENST00000376237.8:c.*580_*581insTTGTT	ENSP00000365412.4:n.*580_*581insTTGTT
ENST00000383329.7:c.993_994insTTGTT	ENSP00000372819.3:p.Met332LeufsTer?
ENST00000470363.5:n.311_312insTTGTT
ENST00000487245.5:n.1352_1353insTTGTT
NM_002117.5:c.993_994insTTGTT	NP_002108.4:p.Met332LeufsTer?
NM_002117.6:c.993_994insTTGTT MANE Select	NP_002108.4:p.Met332LeufsTer?