Canonical Allele Identifier: CA2770490847
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269551_31269552insT , CM000668.2:g.31269551_31269552insT GRCh38
NC_000006.11:g.31237328_31237329insT , CM000668.1:g.31237328_31237329insT GRCh37
NC_000006.10:g.31345307_31345308insT NCBI36
NG_029422.2:g.7580_7581insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1016-27_1016-26insA MANE Select ENSP00000365402.5:n.1016-27_1016-26insA
ENST00000376228.9:c.1016-27_1016-26insA ENSP00000365402.5:n.1016-27_1016-26insA
ENST00000376237.8:c.*603-27_*603-26insA ENSP00000365412.4:n.*603-27_*603-26insA
ENST00000383329.7:c.1016-9_1016-8insA ENSP00000372819.3:n.1016-9_1016-8insA
ENST00000466892.5:n.115_116insA
ENST00000470363.5:n.747_748insA
ENST00000487245.5:n.1375-27_1375-26insA
NM_002117.5:c.1016-27_1016-26insA NP_002108.4:n.1016-27_1016-26insA
NM_002117.6:c.1016-27_1016-26insA MANE Select NP_002108.4:n.1016-27_1016-26insA