Canonical Allele Identifier: CA63898525

Gene: CASP8

Linked Data

• dbSNP Id: rs1052461186
• gnomAD v3: 2-201287893-CTTCTT-C
• gnomAD v4: 2-201287893-CTTCTT-C
• MyVariant Identifiers: chr2:g.202152617_202152621del (hg19) ; chr2:g.201287894_201287898del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201287896_201287900del , CM000664.2:g.201287896_201287900del	GRCh38
NC_000002.11:g.202152619_202152623del , CM000664.1:g.202152619_202152623del	GRCh37
NC_000002.10:g.201860864_201860868del	NCBI36
NG_007497.1:g.59439_59443del , LRG_34:g.59439_59443del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696069.1:c.1259+2579_1259+2583del	ENSP00000512371.1:n.1259+2579_1259+2583del