Canonical Allele Identifier: CA1519173495

Gene: CASP3

Linked Data

• dbSNP Id: rs556569540

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.184627828A>C , CM000666.2:g.184627828A>C	GRCh38
NC_000004.11:g.185548982A>C , CM000666.1:g.185548982A>C	GRCh37
NC_000004.10:g.185785976A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000700100.1:c.*1444T>G	ENSP00000514797.1:n.*1444T>G
ENST00000700101.1:c.*1444T>G	ENSP00000514798.1:n.*1444T>G
ENST00000700102.1:n.3881T>G
ENST00000700103.1:n.5243T>G
ENST00000700104.1:c.*2027T>G	ENSP00000514799.1:n.*2027T>G
ENST00000308394.9:c.*1444T>G MANE Select	ENSP00000311032.4:n.*1444T>G
ENST00000308394.8:c.*1444T>G	ENSP00000311032.4:n.*1444T>G
ENST00000393585.6:c.*1608T>G	ENSP00000377210.2:n.*1608T>G
ENST00000523916.5:c.*1444T>G	ENSP00000428929.1:n.*1444T>G
ENST00000613118.4:c.*1711T>G	ENSP00000478339.1:n.*1711T>G
NM_004346.3:c.*1444T>G	NP_004337.2:n.*1444T>G
NM_032991.2:c.*1444T>G	NP_116786.1:n.*1444T>G
XM_011532301.1:c.*1444T>G	XP_011530603.1:n.*1444T>G
NM_001354777.1:c.*1444T>G	NP_001341706.1:n.*1444T>G
NM_001354779.1:c.*1444T>G	NP_001341708.1:n.*1444T>G
NM_001354780.1:c.*1444T>G	NP_001341709.1:n.*1444T>G
NM_001354781.1:c.*1608T>G	NP_001341710.1:n.*1608T>G
NM_001354782.1:c.*1608T>G	NP_001341711.1:n.*1608T>G
NM_001354783.1:c.*1608T>G	NP_001341712.1:n.*1608T>G
NM_001354784.1:c.*1608T>G	NP_001341713.1:n.*1608T>G
NM_004346.4:c.*1444T>G MANE Select	NP_004337.2:n.*1444T>G
NM_001354777.2:c.*1444T>G	NP_001341706.1:n.*1444T>G
NM_001354779.2:c.*1444T>G	NP_001341708.1:n.*1444T>G
NM_001354780.2:c.*1444T>G	NP_001341709.1:n.*1444T>G
NM_001354781.2:c.*1608T>G	NP_001341710.1:n.*1608T>G
NM_001354782.2:c.*1608T>G	NP_001341711.1:n.*1608T>G
NM_001354783.2:c.*1608T>G	NP_001341712.1:n.*1608T>G
NM_001354784.2:c.*1608T>G	NP_001341713.1:n.*1608T>G
NM_032991.3:c.*1444T>G	NP_116786.1:n.*1444T>G