Canonical Allele Identifier: CA1320996735
Gene: CASP8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201287723_201287724delinsAT , CM000664.2:g.201287723_201287724delinsAT GRCh38
NC_000002.11:g.202152446_202152447delinsAT , CM000664.1:g.202152446_202152447delinsAT GRCh37
NC_000002.10:g.201860691_201860692delinsAT NCBI36
NG_007497.1:g.59266_59267delinsAT , LRG_34:g.59266_59267delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000696069.1:c.1259+2406_1259+2407delinsAT ENSP00000512371.1:n.1259+2406_1259+2407delinsAT