Canonical Allele Identifier: CA2677951052
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31270825-GT-G
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270826del , CM000668.2:g.31270826del GRCh38
NC_000006.11:g.31238603del , CM000668.1:g.31238603del GRCh37
NC_000006.10:g.31346582del NCBI36
NG_029422.2:g.6306del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.619+247del MANE Select ENSP00000365402.5:n.619+247del
ENST00000376228.9:c.619+247del ENSP00000365402.5:n.619+247del
ENST00000376237.8:c.*206+247del ENSP00000365412.4:n.*206+247del
ENST00000383329.7:c.619+247del ENSP00000372819.3:n.619+247del
ENST00000415537.1:c.617+247del
ENST00000487245.5:n.978+247del
ENST00000495835.1:n.808+247del
NM_002117.5:c.619+247del NP_002108.4:n.619+247del
NM_002117.6:c.619+247del MANE Select NP_002108.4:n.619+247del
Search 100 bp 5'
Search 100 bp 3'