Canonical Allele Identifier: CA2677950944
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270707_31270708insTA , CM000668.2:g.31270707_31270708insTA GRCh38
NC_000006.11:g.31238484_31238485insTA , CM000668.1:g.31238484_31238485insTA GRCh37
NC_000006.10:g.31346463_31346464insTA NCBI36
NG_029422.2:g.6424_6425insTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.620-223_620-222insTA MANE Select ENSP00000365402.5:n.620-223_620-222insTA
ENST00000376228.9:c.620-223_620-222insTA ENSP00000365402.5:n.620-223_620-222insTA
ENST00000376237.8:c.*207-223_*207-222insTA ENSP00000365412.4:n.*207-223_*207-222insTA
ENST00000383329.7:c.620-223_620-222insTA ENSP00000372819.3:n.620-223_620-222insTA
ENST00000415537.1:c.618-223_618-222insTA
ENST00000487245.5:n.979-223_979-222insTA
ENST00000495835.1:n.809-223_809-222insTA
NM_002117.5:c.620-223_620-222insTA NP_002108.4:n.620-223_620-222insTA
NM_002117.6:c.620-223_620-222insTA MANE Select NP_002108.4:n.620-223_620-222insTA