Canonical Allele Identifier: CA3051384130

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269989_31269990insCAAAAGCCA , CM000668.2:g.31269989_31269990insCAAAAGCCA	GRCh38
NC_000006.11:g.31237766_31237767insCAAAAGCCA , CM000668.1:g.31237766_31237767insCAAAAGCCA	GRCh37
NC_000006.10:g.31345745_31345746insCAAAAGCCA	NCBI36
NG_029422.2:g.7144_7145insGCTTTTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.993_994insGCTTTTGTG MANE Select	ENSP00000365402.5:p.Met331_Met332insAlaPheVal
ENST00000376228.9:c.993_994insGCTTTTGTG	ENSP00000365402.5:p.Met331_Met332insAlaPheVal
ENST00000376237.8:c.*580_*581insGCTTTTGTG	ENSP00000365412.4:n.*580_*581insGCTTTTGTG
ENST00000383329.7:c.993_994insGCTTTTGTG	ENSP00000372819.3:p.Met331_Met332insAlaPheVal
ENST00000470363.5:n.311_312insGCTTTTGTG
ENST00000487245.5:n.1352_1353insGCTTTTGTG
NM_002117.5:c.993_994insGCTTTTGTG	NP_002108.4:p.Met331_Met332insAlaPheVal
NM_002117.6:c.993_994insGCTTTTGTG MANE Select	NP_002108.4:p.Met331_Met332insAlaPheVal