Canonical Allele Identifier: CA1519173354

Gene: CASP3

Linked Data

• dbSNP Id: rs1741802011

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.184627733G>A , CM000666.2:g.184627733G>A	GRCh38
NC_000004.11:g.185548887G>A , CM000666.1:g.185548887G>A	GRCh37
NC_000004.10:g.185785881G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000700100.1:c.*1539C>T	ENSP00000514797.1:n.*1539C>T
ENST00000700101.1:c.*1539C>T	ENSP00000514798.1:n.*1539C>T
ENST00000700102.1:n.3976C>T
ENST00000700103.1:n.5338C>T
ENST00000700104.1:c.*2122C>T	ENSP00000514799.1:n.*2122C>T
ENST00000308394.9:c.*1539C>T MANE Select	ENSP00000311032.4:n.*1539C>T
ENST00000308394.8:c.*1539C>T	ENSP00000311032.4:n.*1539C>T
ENST00000393585.6:c.*1703C>T	ENSP00000377210.2:n.*1703C>T
ENST00000523916.5:c.*1539C>T	ENSP00000428929.1:n.*1539C>T
ENST00000613118.4:c.*1806C>T	ENSP00000478339.1:n.*1806C>T
NM_004346.3:c.*1539C>T	NP_004337.2:n.*1539C>T
NM_032991.2:c.*1539C>T	NP_116786.1:n.*1539C>T
XM_011532301.1:c.*1539C>T	XP_011530603.1:n.*1539C>T
NM_001354777.1:c.*1539C>T	NP_001341706.1:n.*1539C>T
NM_001354779.1:c.*1539C>T	NP_001341708.1:n.*1539C>T
NM_001354780.1:c.*1539C>T	NP_001341709.1:n.*1539C>T
NM_001354781.1:c.*1703C>T	NP_001341710.1:n.*1703C>T
NM_001354782.1:c.*1703C>T	NP_001341711.1:n.*1703C>T
NM_001354783.1:c.*1703C>T	NP_001341712.1:n.*1703C>T
NM_001354784.1:c.*1703C>T	NP_001341713.1:n.*1703C>T
NM_004346.4:c.*1539C>T MANE Select	NP_004337.2:n.*1539C>T
NM_001354777.2:c.*1539C>T	NP_001341706.1:n.*1539C>T
NM_001354779.2:c.*1539C>T	NP_001341708.1:n.*1539C>T
NM_001354780.2:c.*1539C>T	NP_001341709.1:n.*1539C>T
NM_001354781.2:c.*1703C>T	NP_001341710.1:n.*1703C>T
NM_001354782.2:c.*1703C>T	NP_001341711.1:n.*1703C>T
NM_001354783.2:c.*1703C>T	NP_001341712.1:n.*1703C>T
NM_001354784.2:c.*1703C>T	NP_001341713.1:n.*1703C>T
NM_032991.3:c.*1539C>T	NP_116786.1:n.*1539C>T