Canonical Allele Identifier: CA2677951160
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271025_31271026del , CM000668.2:g.31271025_31271026del GRCh38
NC_000006.11:g.31238802_31238803del , CM000668.1:g.31238802_31238803del GRCh37
NC_000006.10:g.31346781_31346782del NCBI36
NG_029422.2:g.6107_6108del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.619+48_619+49del MANE Select ENSP00000365402.5:n.619+48_619+49del
ENST00000376228.9:c.619+48_619+49del ENSP00000365402.5:n.619+48_619+49del
ENST00000376237.8:c.*206+48_*206+49del ENSP00000365412.4:n.*206+48_*206+49del
ENST00000383329.7:c.619+48_619+49del ENSP00000372819.3:n.619+48_619+49del
ENST00000415537.1:c.617+48_617+49del
ENST00000487245.5:n.978+48_978+49del
ENST00000495835.1:n.808+48_808+49del
NM_002117.5:c.619+48_619+49del NP_002108.4:n.619+48_619+49del
NM_002117.6:c.619+48_619+49del MANE Select NP_002108.4:n.619+48_619+49del