Canonical Allele Identifier: CA1320996837
Gene: CASP8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201287964_201287967delinsCCTT , CM000664.2:g.201287964_201287967delinsCCTT GRCh38
NC_000002.11:g.202152687_202152690delinsCCTT , CM000664.1:g.202152687_202152690delinsCCTT GRCh37
NC_000002.10:g.201860932_201860935delinsCCTT NCBI36
NG_007497.1:g.59507_59510delinsCCTT , LRG_34:g.59507_59510delinsCCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000696069.1:c.1259+2647_1259+2650delinsCCTT ENSP00000512371.1:n.1259+2647_1259+2650delinsCCTT