Canonical Allele Identifier: CA1519174986

Gene: CASP3

Linked Data

• dbSNP Id: rs1579182612
• gnomAD v4: 4-184628885-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.184628885G>T , CM000666.2:g.184628885G>T	GRCh38
NC_000004.11:g.185550039G>T , CM000666.1:g.185550039G>T	GRCh37
NC_000004.10:g.185787033G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700100.1:c.*387C>A	ENSP00000514797.1:n.*387C>A
ENST00000700101.1:c.*387C>A	ENSP00000514798.1:n.*387C>A
ENST00000700102.1:n.2824C>A
ENST00000700103.1:n.4186C>A
ENST00000700104.1:c.*970C>A	ENSP00000514799.1:n.*970C>A
ENST00000308394.9:c.*387C>A MANE Select	ENSP00000311032.4:n.*387C>A
ENST00000308394.8:c.*387C>A	ENSP00000311032.4:n.*387C>A
ENST00000393585.6:c.*551C>A	ENSP00000377210.2:n.*551C>A
ENST00000523916.5:c.*387C>A	ENSP00000428929.1:n.*387C>A
ENST00000613118.4:c.*654C>A	ENSP00000478339.1:n.*654C>A
NM_004346.3:c.*387C>A	NP_004337.2:n.*387C>A
NM_032991.2:c.*387C>A	NP_116786.1:n.*387C>A
XM_011532301.1:c.*387C>A	XP_011530603.1:n.*387C>A
NM_001354777.1:c.*387C>A	NP_001341706.1:n.*387C>A
NM_001354779.1:c.*387C>A	NP_001341708.1:n.*387C>A
NM_001354780.1:c.*387C>A	NP_001341709.1:n.*387C>A
NM_001354781.1:c.*551C>A	NP_001341710.1:n.*551C>A
NM_001354782.1:c.*551C>A	NP_001341711.1:n.*551C>A
NM_001354783.1:c.*551C>A	NP_001341712.1:n.*551C>A
NM_001354784.1:c.*551C>A	NP_001341713.1:n.*551C>A
NM_004346.4:c.*387C>A MANE Select	NP_004337.2:n.*387C>A
NM_001354777.2:c.*387C>A	NP_001341706.1:n.*387C>A
NM_001354779.2:c.*387C>A	NP_001341708.1:n.*387C>A
NM_001354780.2:c.*387C>A	NP_001341709.1:n.*387C>A
NM_001354781.2:c.*551C>A	NP_001341710.1:n.*551C>A
NM_001354782.2:c.*551C>A	NP_001341711.1:n.*551C>A
NM_001354783.2:c.*551C>A	NP_001341712.1:n.*551C>A
NM_001354784.2:c.*551C>A	NP_001341713.1:n.*551C>A
NM_032991.3:c.*387C>A	NP_116786.1:n.*387C>A