Canonical Allele Identifier: CA2677951166
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271036_31271037insCG , CM000668.2:g.31271036_31271037insCG GRCh38
NC_000006.11:g.31238813_31238814insCG , CM000668.1:g.31238813_31238814insCG GRCh37
NC_000006.10:g.31346792_31346793insCG NCBI36
NG_029422.2:g.6095_6096insCG

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.619+36_619+37insCG MANE Select ENSP00000365402.5:n.619+36_619+37insCG
ENST00000376228.9:c.619+36_619+37insCG ENSP00000365402.5:n.619+36_619+37insCG
ENST00000376237.8:c.*206+36_*206+37insCG ENSP00000365412.4:n.*206+36_*206+37insCG
ENST00000383329.7:c.619+36_619+37insCG ENSP00000372819.3:n.619+36_619+37insCG
ENST00000415537.1:c.617+36_617+37insCG
ENST00000487245.5:n.978+36_978+37insCG
ENST00000495835.1:n.808+36_808+37insCG
NM_002117.5:c.619+36_619+37insCG NP_002108.4:n.619+36_619+37insCG
NM_002117.6:c.619+36_619+37insCG MANE Select NP_002108.4:n.619+36_619+37insCG