Canonical Allele Identifier: CA1320996811
Gene: CASP8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201287893_201287898delinsCTTCTT , CM000664.2:g.201287893_201287898delinsCTTCTT GRCh38
NC_000002.11:g.202152616_202152621delinsCTTCTT , CM000664.1:g.202152616_202152621delinsCTTCTT GRCh37
NC_000002.10:g.201860861_201860866delinsCTTCTT NCBI36
NG_007497.1:g.59436_59441delinsCTTCTT , LRG_34:g.59436_59441delinsCTTCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000696069.1:c.1259+2576_1259+2581delinsCTTCTT ENSP00000512371.1:n.1259+2576_1259+2581delinsCTTCTT