Canonical Allele Identifier: CA2840984778

Gene: CASP10

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201187862C>T , CM000664.2:g.201187862C>T	GRCh38
NC_000002.11:g.202052585C>T , CM000664.1:g.202052585C>T	GRCh37
NC_000002.10:g.201760830C>T	NCBI36
NG_007265.1:g.9731C>T , LRG_33:g.9731C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.441+63C>T	ENSP00000314599.7:n.441+63C>T
ENST00000346817.10:c.441+63C>T	ENSP00000237865.7:n.441+63C>T
ENST00000374650.8:c.441+63C>T	ENSP00000363781.3:n.441+63C>T
ENST00000438843.6:c.347+1738C>T	ENSP00000401914.1:n.347+1738C>T
ENST00000471191.2:c.441+63C>T	ENSP00000512475.1:n.441+63C>T
ENST00000485408.2:n.876+63C>T
ENST00000492363.6:c.441+63C>T	ENSP00000512459.1:n.441+63C>T
ENST00000696190.1:n.679C>T
ENST00000696191.1:n.765+1738C>T
ENST00000696199.1:c.441+63C>T	ENSP00000512481.1:n.441+63C>T
ENST00000286186.11:c.441+63C>T MANE Select	ENSP00000286186.6:n.441+63C>T
ENST00000272879.9:c.441+63C>T	ENSP00000272879.5:n.441+63C>T
ENST00000286186.10:c.441+63C>T	ENSP00000286186.6:n.441+63C>T
ENST00000313728.11:c.441+63C>T	ENSP00000314599.7:n.441+63C>T
ENST00000346817.9:c.441+63C>T	ENSP00000237865.7:n.441+63C>T
ENST00000360132.7:c.441+63C>T	ENSP00000353250.3:n.441+63C>T
ENST00000374650.7:c.441+63C>T	ENSP00000363781.3:n.441+63C>T
ENST00000438843.5:c.347+1738C>T	ENSP00000401914.1:n.347+1738C>T
ENST00000448480.1:c.441+63C>T	ENSP00000396835.1:n.441+63C>T
ENST00000460140.5:n.645+63C>T
ENST00000471191.1:n.120+63C>T
ENST00000485408.1:n.54+63C>T
ENST00000492363.5:n.441+63C>T
NM_001206524.1:c.441+63C>T	NP_001193453.1:n.441+63C>T
NM_001206542.1:c.441+63C>T	NP_001193471.1:n.441+63C>T
NM_001230.4:c.441+63C>T	NP_001221.2:n.441+63C>T
NM_001306083.1:c.441+63C>T	NP_001293012.1:n.441+63C>T
NM_032974.4:c.441+63C>T	NP_116756.2:n.441+63C>T
NM_032976.3:c.441+63C>T	NP_116758.1:n.441+63C>T
NM_032977.3:c.441+63C>T , LRG_33t1:c.441+63C>T	NP_116759.2:n.441+63C>T
XM_005246907.2:c.441+63C>T	XP_005246964.1:n.441+63C>T
XM_006712796.2:c.-215+63C>T	XP_006712859.1:n.-215+63C>T
XM_011511990.1:c.441+63C>T	XP_011510292.1:n.441+63C>T
XR_923043.1:n.645+63C>T
XR_923044.1:n.645+63C>T
XM_006712796.3:c.-215+63C>T	XP_006712859.1:n.-215+63C>T
XM_011511990.2:c.441+63C>T	XP_011510292.1:n.441+63C>T
XR_923043.2:n.645+63C>T
XR_923044.2:n.645+63C>T
NM_001206524.2:c.441+63C>T	NP_001193453.1:n.441+63C>T
NM_001206542.2:c.441+63C>T	NP_001193471.1:n.441+63C>T
NM_001230.5:c.441+63C>T	NP_001221.2:n.441+63C>T
NM_001306083.2:c.441+63C>T	NP_001293012.1:n.441+63C>T
NM_032974.5:c.441+63C>T	NP_116756.2:n.441+63C>T
NM_032977.4:c.441+63C>T MANE Select	NP_116759.2:n.441+63C>T
NM_032976.4:c.441+63C>T	NP_116758.1:n.441+63C>T