Canonical Allele Identifier: CA11741617

Gene: CASP3

Identifiers and link-outs to other resources

• dbSNP Id: rs4647610
• gnomAD: 4:185567931 C / T
• MyVariant Identifiers: chr4:g.185567931C>T (hg19) ; chr4:g.184646777C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.184646777C>T , CM000666.2:g.184646777C>T	GRCh38
NC_000004.11:g.185567931C>T , CM000666.1:g.185567931C>T	GRCh37
NC_000004.10:g.185804925C>T	NCBI36
NG_051582.1:g.2165C>T

Transcript Alleles

HGVS	Amino-acid change
NM_004346.3:c.-16+1688G>A VV	NP_004337.2:p.=
NM_032991.2:c.-16+2618G>A VV	NP_116786.1:p.=
XM_011532301.1:c.-16+1726G>A	XP_011530603.1:p.=
NM_001354777.1:c.-16+1726G>A VV	NP_001341706.1:p.=
NM_001354779.1:c.-90+2618G>A VV	NP_001341708.1:p.=
NM_001354780.1:c.-90+1688G>A VV	NP_001341709.1:p.=
NM_001354781.1:c.-16+2618G>A VV	NP_001341710.1:p.=
NM_001354782.1:c.-16+1688G>A VV	NP_001341711.1:p.=
NM_001354783.1:c.-181+1688G>A VV	NP_001341712.1:p.=
NM_001354784.1:c.-90+2618G>A VV	NP_001341713.1:p.=
NM_004346.4:c.-16+1688G>A VV MANE Preferred	NP_004337.2:p.=
NM_001354777.2:c.-16+1726G>A VV	NP_001341706.1:p.=
NM_001354779.2:c.-90+2618G>A VV	NP_001341708.1:p.=
NM_001354780.2:c.-90+1688G>A VV	NP_001341709.1:p.=
NM_001354781.2:c.-16+2618G>A VV	NP_001341710.1:p.=
NM_001354782.2:c.-16+1688G>A VV	NP_001341711.1:p.=
NM_001354783.2:c.-181+1688G>A VV	NP_001341712.1:p.=
NM_001354784.2:c.-90+2618G>A VV	NP_001341713.1:p.=
NM_032991.3:c.-16+2618G>A VV	NP_116786.1:p.=
ENST00000308394.8:c.-16+1688G>A	ENSP00000311032.4:p.=
ENST00000393585.6:c.-208+1688G>A	ENSP00000377210.2:p.=
ENST00000393588.8:c.-16+2618G>A	ENSP00000377213.4:p.=
ENST00000447121.2:c.-16+1726G>A	ENSP00000407142.2:p.=
ENST00000517513.5:c.-16+1688G>A	ENSP00000428372.1:p.=
ENST00000523916.5:c.-16+2618G>A	ENSP00000428929.1:p.=
ENST00000613118.4:c.-181+1688G>A	ENSP00000478339.1:p.=