Canonical Allele Identifier: CA430612430

Gene: CASP10

Linked Data

• MyVariant Identifiers: chr2:g.202072899A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201208176A>G , CM000664.2:g.201208176A>G	GRCh38
NC_000002.11:g.202072899A>G , CM000664.1:g.202072899A>G	GRCh37
NC_000002.10:g.201781144A>G	NCBI36
NG_007265.1:g.30045A>G , LRG_33:g.30045A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.722-894A>G	ENSP00000314599.7:n.722-894A>G
ENST00000346817.10:c.786A>G	ENSP00000237865.7:p.Lys262=
ENST00000438843.6:c.*372A>G	ENSP00000401914.1:n.*372A>G
ENST00000492363.6:c.*1A>G	ENSP00000512459.1:n.*1A>G
ENST00000696199.1:c.721+4410A>G	ENSP00000512481.1:n.721+4410A>G
ENST00000286186.11:c.915A>G MANE Select	ENSP00000286186.6:p.Lys305=
ENST00000272879.9:c.915A>G	ENSP00000272879.5:p.Lys305=
ENST00000286186.10:c.915A>G	ENSP00000286186.6:p.Lys305=
ENST00000313728.11:c.722-894A>G	ENSP00000314599.7:n.722-894A>G
ENST00000346817.9:c.786A>G	ENSP00000237865.7:p.Lys262=
ENST00000360132.7:c.*1A>G	ENSP00000353250.3:n.*1A>G
ENST00000448480.1:c.786A>G	ENSP00000396835.1:p.Lys262=
ENST00000492363.5:n.823A>G
NM_001206524.1:c.722-894A>G	NP_001193453.1:n.722-894A>G
NM_001206542.1:c.786A>G	NP_001193471.1:p.Lys262=
NM_001230.4:c.786A>G	NP_001221.2:p.Lys262=
NM_032974.4:c.915A>G	NP_116756.2:p.Lys305=
NM_032976.3:c.*1A>G	NP_116758.1:n.*1A>G
NM_032977.3:c.915A>G , LRG_33t1:c.915A>G	NP_116759.2:p.Lys305=
XM_005246907.2:c.912A>G	XP_005246964.1:p.Lys304=
XM_006712796.2:c.165A>G	XP_006712859.1:p.Lys55=
XM_011511990.1:c.*1A>G	XP_011510292.1:n.*1A>G
XR_923043.1:n.1119A>G
XR_923044.1:n.1027A>G
XM_006712796.3:c.165A>G	XP_006712859.1:p.Lys55=
XM_011511990.2:c.*1A>G	XP_011510292.1:n.*1A>G
XR_923043.2:n.1119A>G
XR_923044.2:n.1027A>G
NM_001206524.2:c.722-894A>G	NP_001193453.1:n.722-894A>G
NM_001206542.2:c.786A>G	NP_001193471.1:p.Lys262=
NM_001230.5:c.786A>G	NP_001221.2:p.Lys262=
NM_032974.5:c.915A>G	NP_116756.2:p.Lys305=
NM_032977.4:c.915A>G MANE Select	NP_116759.2:p.Lys305=
NM_032976.4:c.*1A>G	NP_116758.1:n.*1A>G