Canonical Allele Identifier: CA2672813045

Gene: CASP3

Linked Data

• gnomAD v4: 4-184648510-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.184648510C>A , CM000666.2:g.184648510C>A	GRCh38
NC_000004.11:g.185569664C>A , CM000666.1:g.185569664C>A	GRCh37
NC_000004.10:g.185806658C>A	NCBI36
NG_051582.1:g.3898C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000700100.1:c.-61G>T	ENSP00000514797.1:n.-61G>T
ENST00000700101.1:c.-16+1482G>T	ENSP00000514798.1:n.-16+1482G>T
ENST00000700102.1:n.53+885G>T
ENST00000700103.1:n.53+885G>T
ENST00000700104.1:c.-16+885G>T	ENSP00000514799.1:n.-16+885G>T
ENST00000308394.9:c.-61G>T MANE Select	ENSP00000311032.4:n.-61G>T
ENST00000308394.8:c.-61G>T	ENSP00000311032.4:n.-61G>T
ENST00000393585.6:c.-253G>T	ENSP00000377210.2:n.-253G>T
ENST00000393588.8:c.-16+885G>T	ENSP00000377213.4:n.-16+885G>T
ENST00000447121.2:c.-23G>T	ENSP00000407142.2:n.-23G>T
ENST00000517513.5:c.-61G>T	ENSP00000428372.1:n.-61G>T
ENST00000523916.5:c.-16+885G>T	ENSP00000428929.1:n.-16+885G>T
ENST00000613118.4:c.-226G>T	ENSP00000478339.1:n.-226G>T
NM_004346.3:c.-61G>T	NP_004337.2:n.-61G>T
NM_032991.2:c.-16+885G>T	NP_116786.1:n.-16+885G>T
XM_011532301.1:c.-23G>T	XP_011530603.1:n.-23G>T
NM_001354777.1:c.-23G>T	NP_001341706.1:n.-23G>T
NM_001354779.1:c.-90+885G>T	NP_001341708.1:n.-90+885G>T
NM_001354780.1:c.-135G>T	NP_001341709.1:n.-135G>T
NM_001354781.1:c.-16+885G>T	NP_001341710.1:n.-16+885G>T
NM_001354782.1:c.-61G>T	NP_001341711.1:n.-61G>T
NM_001354783.1:c.-226G>T	NP_001341712.1:n.-226G>T
NM_001354784.1:c.-90+885G>T	NP_001341713.1:n.-90+885G>T
NM_004346.4:c.-61G>T MANE Select	NP_004337.2:n.-61G>T
NM_001354777.2:c.-23G>T	NP_001341706.1:n.-23G>T
NM_001354779.2:c.-90+885G>T	NP_001341708.1:n.-90+885G>T
NM_001354780.2:c.-135G>T	NP_001341709.1:n.-135G>T
NM_001354781.2:c.-16+885G>T	NP_001341710.1:n.-16+885G>T
NM_001354782.2:c.-61G>T	NP_001341711.1:n.-61G>T
NM_001354783.2:c.-226G>T	NP_001341712.1:n.-226G>T
NM_001354784.2:c.-90+885G>T	NP_001341713.1:n.-90+885G>T
NM_032991.3:c.-16+885G>T	NP_116786.1:n.-16+885G>T