Canonical Allele Identifier: CA792193880

Gene: CASP3

Linked Data

• dbSNP Id: rs1195833992
• MyVariant Identifiers: chr4:g.185548862T>C (hg19) ; chr4:g.184627708T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.184627708T>C , CM000666.2:g.184627708T>C	GRCh38
NC_000004.11:g.185548862T>C , CM000666.1:g.185548862T>C	GRCh37
NC_000004.10:g.185785856T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000700100.1:c.*1564A>G	ENSP00000514797.1:n.*1564A>G
ENST00000700101.1:c.*1564A>G	ENSP00000514798.1:n.*1564A>G
ENST00000700102.1:n.4001A>G
ENST00000308394.9:c.*1564A>G MANE Select	ENSP00000311032.4:n.*1564A>G
ENST00000308394.8:c.*1564A>G	ENSP00000311032.4:n.*1564A>G
ENST00000393585.6:c.*1728A>G	ENSP00000377210.2:n.*1728A>G
ENST00000523916.5:c.*1564A>G	ENSP00000428929.1:n.*1564A>G
ENST00000613118.4:c.*1831A>G	ENSP00000478339.1:n.*1831A>G
NM_004346.3:c.*1564A>G	NP_004337.2:n.*1564A>G
NM_032991.2:c.*1564A>G	NP_116786.1:n.*1564A>G
XM_011532301.1:c.*1564A>G	XP_011530603.1:n.*1564A>G
NM_001354777.1:c.*1564A>G	NP_001341706.1:n.*1564A>G
NM_001354779.1:c.*1564A>G	NP_001341708.1:n.*1564A>G
NM_001354780.1:c.*1564A>G	NP_001341709.1:n.*1564A>G
NM_001354781.1:c.*1728A>G	NP_001341710.1:n.*1728A>G
NM_001354782.1:c.*1728A>G	NP_001341711.1:n.*1728A>G
NM_001354783.1:c.*1728A>G	NP_001341712.1:n.*1728A>G
NM_001354784.1:c.*1728A>G	NP_001341713.1:n.*1728A>G
NM_004346.4:c.*1564A>G MANE Select	NP_004337.2:n.*1564A>G
NM_001354777.2:c.*1564A>G	NP_001341706.1:n.*1564A>G
NM_001354779.2:c.*1564A>G	NP_001341708.1:n.*1564A>G
NM_001354780.2:c.*1564A>G	NP_001341709.1:n.*1564A>G
NM_001354781.2:c.*1728A>G	NP_001341710.1:n.*1728A>G
NM_001354782.2:c.*1728A>G	NP_001341711.1:n.*1728A>G
NM_001354783.2:c.*1728A>G	NP_001341712.1:n.*1728A>G
NM_001354784.2:c.*1728A>G	NP_001341713.1:n.*1728A>G
NM_032991.3:c.*1564A>G	NP_116786.1:n.*1564A>G