Canonical Allele Identifier: CA1619079591
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270250_31270252delinsCAT , CM000668.2:g.31270250_31270252delinsCAT GRCh38
NC_000006.11:g.31238027_31238029delinsCAT , CM000668.1:g.31238027_31238029delinsCAT GRCh37
NC_000006.10:g.31346006_31346008delinsCAT NCBI36
NG_029422.2:g.6880_6882delinsATG

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.853_855delinsATG MANE Select ENSP00000365402.5:p.Met285=
ENST00000376228.9:c.853_855delinsATG ENSP00000365402.5:p.Met285=
ENST00000376237.8:c.*440_*442delinsATG ENSP00000365412.4:n.*440_*442delinsATG
ENST00000383329.7:c.853_855delinsATG ENSP00000372819.3:p.Met285=
ENST00000415537.1:c.744_746delinsATG
ENST00000470363.5:n.171_173delinsATG
ENST00000487245.5:n.1212_1214delinsATG
ENST00000495835.1:n.1042_1044delinsATG
NM_002117.5:c.853_855delinsATG NP_002108.4:p.Met285=
NM_002117.6:c.853_855delinsATG MANE Select NP_002108.4:p.Met285=