Canonical Allele Identifier: CA2677951605
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271531_31271532insT , CM000668.2:g.31271531_31271532insT GRCh38
NC_000006.11:g.31239308_31239309insT , CM000668.1:g.31239308_31239309insT GRCh37
NC_000006.10:g.31347287_31347288insT NCBI36
NG_029422.2:g.5600_5601insA

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.343+67_343+68insA MANE Select ENSP00000365402.5:n.343+67_343+68insA
ENST00000376228.9:c.343+67_343+68insA ENSP00000365402.5:n.343+67_343+68insA
ENST00000376237.8:c.343+67_343+68insA ENSP00000365412.4:n.343+67_343+68insA
ENST00000383329.7:c.343+67_343+68insA ENSP00000372819.3:n.343+67_343+68insA
ENST00000415537.1:c.341+67_341+68insA
ENST00000484378.1:n.429_430insA
ENST00000487245.5:n.519_520insA
ENST00000495835.1:n.532+67_532+68insA
NM_002117.5:c.343+67_343+68insA NP_002108.4:n.343+67_343+68insA
NM_002117.6:c.343+67_343+68insA MANE Select NP_002108.4:n.343+67_343+68insA