Canonical Allele Identifier: CA430829594

Gene: CASP10

Linked Data

• gnomAD v4: 2-201209386-A-G
• MyVariant Identifiers: chr2:g.202074109A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201209386A>G , CM000664.2:g.201209386A>G	GRCh38
NC_000002.11:g.202074109A>G , CM000664.1:g.202074109A>G	GRCh37
NC_000002.10:g.201782354A>G	NCBI36
NG_007265.1:g.31255A>G , LRG_33:g.31255A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.1038A>G	ENSP00000314599.7:p.Glu346=
ENST00000346817.10:c.1110A>G	ENSP00000237865.7:p.Glu370=
ENST00000438843.6:c.*696A>G	ENSP00000401914.1:n.*696A>G
ENST00000492363.6:c.*325A>G	ENSP00000512459.1:n.*325A>G
ENST00000696199.1:c.721+5620A>G	ENSP00000512481.1:n.721+5620A>G
ENST00000286186.11:c.1239A>G MANE Select	ENSP00000286186.6:p.Glu413=
ENST00000272879.9:c.1239A>G	ENSP00000272879.5:p.Glu413=
ENST00000286186.10:c.1239A>G	ENSP00000286186.6:p.Glu413=
ENST00000313728.11:c.1038A>G	ENSP00000314599.7:p.Glu346=
ENST00000346817.9:c.1110A>G	ENSP00000237865.7:p.Glu370=
ENST00000360132.7:c.*325A>G	ENSP00000353250.3:n.*325A>G
ENST00000448480.1:c.1110A>G	ENSP00000396835.1:p.Glu370=
ENST00000492363.5:n.1147A>G
NM_001206524.1:c.1038A>G	NP_001193453.1:p.Glu346=
NM_001206542.1:c.1110A>G	NP_001193471.1:p.Glu370=
NM_001230.4:c.1110A>G	NP_001221.2:p.Glu370=
NM_032974.4:c.1239A>G	NP_116756.2:p.Glu413=
NM_032976.3:c.*325A>G	NP_116758.1:n.*325A>G
NM_032977.3:c.1239A>G , LRG_33t1:c.1239A>G	NP_116759.2:p.Glu413=
XM_005246907.2:c.1236A>G	XP_005246964.1:p.Glu412=
XM_006712796.2:c.489A>G	XP_006712859.1:p.Glu163=
XM_006712796.3:c.489A>G	XP_006712859.1:p.Glu163=
NM_001206524.2:c.1038A>G	NP_001193453.1:p.Glu346=
NM_001206542.2:c.1110A>G	NP_001193471.1:p.Glu370=
NM_001230.5:c.1110A>G	NP_001221.2:p.Glu370=
NM_032974.5:c.1239A>G	NP_116756.2:p.Glu413=
NM_032977.4:c.1239A>G MANE Select	NP_116759.2:p.Glu413=
NM_032976.4:c.*325A>G	NP_116758.1:n.*325A>G