Canonical Allele Identifier: CA2677950201
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269891_31269892insTTAGA , CM000668.2:g.31269891_31269892insTTAGA GRCh38
NC_000006.11:g.31237668_31237669insTTAGA , CM000668.1:g.31237668_31237669insTTAGA GRCh37
NC_000006.10:g.31345647_31345648insTTAGA NCBI36
NG_029422.2:g.7240_7241insTCTAA

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.1015+74_1015+75insTCTAA MANE Select ENSP00000365402.5:n.1015+74_1015+75insTCT...
ENST00000376228.9:c.1015+74_1015+75insTCTAA ENSP00000365402.5:n.1015+74_1015+75insTCT...
ENST00000376237.8:c.*602+74_*602+75insTCTAA ENSP00000365412.4:n.*602+74_*602+75insTCT...
ENST00000383329.7:c.1015+74_1015+75insTCTAA ENSP00000372819.3:n.1015+74_1015+75insTCT...
ENST00000470363.5:n.407_408insTCTAA
ENST00000487245.5:n.1374+74_1374+75insTCTAA
NM_002117.5:c.1015+74_1015+75insTCTAA NP_002108.4:n.1015+74_1015+75insTCTAA
NM_002117.6:c.1015+74_1015+75insTCTAA MANE Select NP_002108.4:n.1015+74_1015+75insTCTAA