Canonical Allele Identifier: CA350291655

Gene: CASP10

Linked Data

• MyVariant Identifiers: chr2:g.202074011T>A (hg19) ; chr2:g.201209288T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201209288T>A , CM000664.2:g.201209288T>A	GRCh38
NC_000002.11:g.202074011T>A , CM000664.1:g.202074011T>A	GRCh37
NC_000002.10:g.201782256T>A	NCBI36
NG_007265.1:g.31157T>A , LRG_33:g.31157T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000313728.12:c.940T>A	ENSP00000314599.7:p.Phe314Ile
ENST00000346817.10:c.1012T>A	ENSP00000237865.7:p.Phe338Ile
ENST00000438843.6:c.*598T>A	ENSP00000401914.1:n.*598T>A
ENST00000492363.6:c.*227T>A	ENSP00000512459.1:n.*227T>A
ENST00000696199.1:c.721+5522T>A	ENSP00000512481.1:n.721+5522T>A
ENST00000286186.11:c.1141T>A MANE Select	ENSP00000286186.6:p.Phe381Ile
ENST00000272879.9:c.1141T>A	ENSP00000272879.5:p.Phe381Ile
ENST00000286186.10:c.1141T>A	ENSP00000286186.6:p.Phe381Ile
ENST00000313728.11:c.940T>A	ENSP00000314599.7:p.Phe314Ile
ENST00000346817.9:c.1012T>A	ENSP00000237865.7:p.Phe338Ile
ENST00000360132.7:c.*227T>A	ENSP00000353250.3:n.*227T>A
ENST00000448480.1:c.1012T>A	ENSP00000396835.1:p.Phe338Ile
ENST00000492363.5:n.1049T>A
NM_001206524.1:c.940T>A	NP_001193453.1:p.Phe314Ile
NM_001206542.1:c.1012T>A	NP_001193471.1:p.Phe338Ile
NM_001230.4:c.1012T>A	NP_001221.2:p.Phe338Ile
NM_032974.4:c.1141T>A	NP_116756.2:p.Phe381Ile
NM_032976.3:c.*227T>A	NP_116758.1:n.*227T>A
NM_032977.3:c.1141T>A , LRG_33t1:c.1141T>A	NP_116759.2:p.Phe381Ile
XM_005246907.2:c.1138T>A	XP_005246964.1:p.Phe380Ile
XM_006712796.2:c.391T>A	XP_006712859.1:p.Phe131Ile
XM_006712796.3:c.391T>A	XP_006712859.1:p.Phe131Ile
NM_001206524.2:c.940T>A	NP_001193453.1:p.Phe314Ile
NM_001206542.2:c.1012T>A	NP_001193471.1:p.Phe338Ile
NM_001230.5:c.1012T>A	NP_001221.2:p.Phe338Ile
NM_032974.5:c.1141T>A	NP_116756.2:p.Phe381Ile
NM_032977.4:c.1141T>A MANE Select	NP_116759.2:p.Phe381Ile
NM_032976.4:c.*227T>A	NP_116758.1:n.*227T>A