Canonical Allele Identifier: CA1519174516
Gene: CASP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.184628703C= , CM000666.2:g.184628703C= GRCh38
NC_000004.11:g.185549857C= , CM000666.1:g.185549857C= GRCh37
NC_000004.10:g.185786851C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000700100.1:c.*569G= ENSP00000514797.1:n.*569G=
ENST00000700101.1:c.*569G= ENSP00000514798.1:n.*569G=
ENST00000700102.1:n.3006G=
ENST00000700103.1:n.4368G=
ENST00000700104.1:c.*1152G= ENSP00000514799.1:n.*1152G=
ENST00000308394.9:c.*569G= MANE Select ENSP00000311032.4:n.*569G=
ENST00000308394.8:c.*569G= ENSP00000311032.4:n.*569G=
ENST00000393585.6:c.*733G= ENSP00000377210.2:n.*733G=
ENST00000523916.5:c.*569G= ENSP00000428929.1:n.*569G=
ENST00000613118.4:c.*836G= ENSP00000478339.1:n.*836G=
NM_004346.3:c.*569G= NP_004337.2:n.*569G=
NM_032991.2:c.*569G= NP_116786.1:n.*569G=
XM_011532301.1:c.*569G= XP_011530603.1:n.*569G=
NM_001354777.1:c.*569G= NP_001341706.1:n.*569G=
NM_001354779.1:c.*569G= NP_001341708.1:n.*569G=
NM_001354780.1:c.*569G= NP_001341709.1:n.*569G=
NM_001354781.1:c.*733G= NP_001341710.1:n.*733G=
NM_001354782.1:c.*733G= NP_001341711.1:n.*733G=
NM_001354783.1:c.*733G= NP_001341712.1:n.*733G=
NM_001354784.1:c.*733G= NP_001341713.1:n.*733G=
NM_004346.4:c.*569G= MANE Select NP_004337.2:n.*569G=
NM_001354777.2:c.*569G= NP_001341706.1:n.*569G=
NM_001354779.2:c.*569G= NP_001341708.1:n.*569G=
NM_001354780.2:c.*569G= NP_001341709.1:n.*569G=
NM_001354781.2:c.*733G= NP_001341710.1:n.*733G=
NM_001354782.2:c.*733G= NP_001341711.1:n.*733G=
NM_001354783.2:c.*733G= NP_001341712.1:n.*733G=
NM_001354784.2:c.*733G= NP_001341713.1:n.*733G=
NM_032991.3:c.*569G= NP_116786.1:n.*569G=