Canonical Allele Identifier: CA2844096462
Gene: HLA-C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271724_31271725insAACGGCG , CM000668.2:g.31271724_31271725insAACGGCG GRCh38
NC_000006.11:g.31239501_31239502insAACGGCG , CM000668.1:g.31239501_31239502insAACGGCG GRCh37
NC_000006.10:g.31347480_31347481insAACGGCG NCBI36
NG_029422.2:g.5413_5414insTCGCCGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.223_224insTCGCCGT MANE Select ENSP00000365402.5:p.Trp75PhefsTer26
ENST00000376228.9:c.223_224insTCGCCGT ENSP00000365402.5:p.Trp75PhefsTer26
ENST00000376237.8:c.223_224insTCGCCGT ENSP00000365412.4:p.Trp75PhefsTer26
ENST00000383329.7:c.223_224insTCGCCGT ENSP00000372819.3:p.Trp75PhefsTer26
ENST00000415537.1:c.221_222insTCGCCGT
ENST00000484378.1:n.242_243insTCGCCGT
ENST00000487245.5:n.332_333insTCGCCGT
ENST00000495835.1:n.412_413insTCGCCGT
NM_002117.5:c.223_224insTCGCCGT NP_002108.4:p.Trp75PhefsTer26
NM_002117.6:c.223_224insTCGCCGT MANE Select NP_002108.4:p.Trp75PhefsTer26
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