Canonical Allele Identifier: CA1519162816

Gene: CASP3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.184649399T= , CM000666.2:g.184649399T=	GRCh38
NC_000004.11:g.185570553T= , CM000666.1:g.185570553T=	GRCh37
NC_000004.10:g.185807547T=	NCBI36
NG_051582.1:g.4787T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700101.1:c.-16+593A=	ENSP00000514798.1:n.-16+593A=
ENST00000700102.1:n.49A=
ENST00000700103.1:n.49A=
ENST00000700104.1:c.-20A=	ENSP00000514799.1:n.-20A=
ENST00000308394.9:c.-187A= MANE Select	ENSP00000311032.4:n.-187A=
ENST00000308394.8:c.-187A=	ENSP00000311032.4:n.-187A=
ENST00000393588.8:c.-20A=	ENSP00000377213.4:n.-20A=
ENST00000447121.2:c.-149A=	ENSP00000407142.2:n.-149A=
ENST00000517513.5:c.-187A=	ENSP00000428372.1:n.-187A=
ENST00000523916.5:c.-20A=	ENSP00000428929.1:n.-20A=
NM_004346.3:c.-187A=	NP_004337.2:n.-187A=
NM_032991.2:c.-20A=	NP_116786.1:n.-20A=
XM_011532301.1:c.-149A=	XP_011530603.1:n.-149A=
NM_001354777.1:c.-149A=	NP_001341706.1:n.-149A=
NM_001354779.1:c.-94A=	NP_001341708.1:n.-94A=
NM_001354780.1:c.-261A=	NP_001341709.1:n.-261A=
NM_001354781.1:c.-20A=	NP_001341710.1:n.-20A=
NM_001354782.1:c.-187A=	NP_001341711.1:n.-187A=
NM_001354783.1:c.-352A=	NP_001341712.1:n.-352A=
NM_001354784.1:c.-94A=	NP_001341713.1:n.-94A=
NM_004346.4:c.-187A= MANE Select	NP_004337.2:n.-187A=
NM_001354777.2:c.-149A=	NP_001341706.1:n.-149A=
NM_001354779.2:c.-94A=	NP_001341708.1:n.-94A=
NM_001354780.2:c.-261A=	NP_001341709.1:n.-261A=
NM_001354781.2:c.-20A=	NP_001341710.1:n.-20A=
NM_001354782.2:c.-187A=	NP_001341711.1:n.-187A=
NM_001354783.2:c.-352A=	NP_001341712.1:n.-352A=
NM_001354784.2:c.-94A=	NP_001341713.1:n.-94A=
NM_032991.3:c.-20A=	NP_116786.1:n.-20A=