Canonical Allele Identifier: CA136862338
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs281860587
MyVariant Identifiers: chr6:g.31237576_31237577insCA (hg19) chr6:g.31269799_31269800insCA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269799_31269800insCA , CM000668.2:g.31269799_31269800insCA GRCh38
NC_000006.11:g.31237576_31237577insCA , CM000668.1:g.31237576_31237577insCA GRCh37
NC_000006.10:g.31345555_31345556insCA NCBI36
NG_029422.2:g.7332_7333insTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1015+166_1015+167insTG MANE Select ENSP00000365402.5:n.1015+166_1015+167insTG
ENST00000376228.9:c.1015+166_1015+167insTG ENSP00000365402.5:n.1015+166_1015+167insTG
ENST00000376237.8:c.*602+166_*602+167insTG ENSP00000365412.4:n.*602+166_*602+167insTG
ENST00000383329.7:c.1015+166_1015+167insTG ENSP00000372819.3:n.1015+166_1015+167insTG
ENST00000470363.5:n.499_500insTG
ENST00000487245.5:n.1374+166_1374+167insTG
NM_002117.5:c.1015+166_1015+167insTG NP_002108.4:n.1015+166_1015+167insTG
NM_002117.6:c.1015+166_1015+167insTG MANE Select NP_002108.4:n.1015+166_1015+167insTG
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