Canonical Allele Identifier: CA350278275

Gene: CASP10

Linked Data

• MyVariant Identifiers: chr2:g.202052497A>G (hg19) ; chr2:g.201187774A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201187774A>G , CM000664.2:g.201187774A>G	GRCh38
NC_000002.11:g.202052497A>G , CM000664.1:g.202052497A>G	GRCh37
NC_000002.10:g.201760742A>G	NCBI36
NG_007265.1:g.9643A>G , LRG_33:g.9643A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.416A>G	ENSP00000314599.7:p.Lys139Arg
ENST00000346817.10:c.416A>G	ENSP00000237865.7:p.Lys139Arg
ENST00000374650.8:c.416A>G	ENSP00000363781.3:p.Lys139Arg
ENST00000438843.6:c.347+1650A>G	ENSP00000401914.1:n.347+1650A>G
ENST00000471191.2:c.416A>G	ENSP00000512475.1:p.Lys139Arg
ENST00000485408.2:n.851A>G
ENST00000492363.6:c.416A>G	ENSP00000512459.1:p.Lys139Arg
ENST00000696190.1:n.591A>G
ENST00000696191.1:n.765+1650A>G
ENST00000696199.1:c.416A>G	ENSP00000512481.1:p.Lys139Arg
ENST00000286186.11:c.416A>G MANE Select	ENSP00000286186.6:p.Lys139Arg
ENST00000272879.9:c.416A>G	ENSP00000272879.5:p.Lys139Arg
ENST00000286186.10:c.416A>G	ENSP00000286186.6:p.Lys139Arg
ENST00000313728.11:c.416A>G	ENSP00000314599.7:p.Lys139Arg
ENST00000346817.9:c.416A>G	ENSP00000237865.7:p.Lys139Arg
ENST00000360132.7:c.416A>G	ENSP00000353250.3:p.Lys139Arg
ENST00000374650.7:c.416A>G	ENSP00000363781.3:p.Lys139Arg
ENST00000438843.5:c.347+1650A>G	ENSP00000401914.1:n.347+1650A>G
ENST00000448480.1:c.416A>G	ENSP00000396835.1:p.Lys139Arg
ENST00000460140.5:n.620A>G
ENST00000471191.1:n.95A>G
ENST00000485408.1:n.29A>G
ENST00000492363.5:n.416A>G
NM_001206524.1:c.416A>G	NP_001193453.1:p.Lys139Arg
NM_001206542.1:c.416A>G	NP_001193471.1:p.Lys139Arg
NM_001230.4:c.416A>G	NP_001221.2:p.Lys139Arg
NM_001306083.1:c.416A>G	NP_001293012.1:p.Lys139Arg
NM_032974.4:c.416A>G	NP_116756.2:p.Lys139Arg
NM_032976.3:c.416A>G	NP_116758.1:p.Lys139Arg
NM_032977.3:c.416A>G , LRG_33t1:c.416A>G	NP_116759.2:p.Lys139Arg
XM_005246907.2:c.416A>G	XP_005246964.1:p.Lys139Arg
XM_006712796.2:c.-240A>G	XP_006712859.1:n.-240A>G
XM_011511990.1:c.416A>G	XP_011510292.1:p.Lys139Arg
XR_923043.1:n.620A>G
XR_923044.1:n.620A>G
XM_006712796.3:c.-240A>G	XP_006712859.1:n.-240A>G
XM_011511990.2:c.416A>G	XP_011510292.1:p.Lys139Arg
XR_923043.2:n.620A>G
XR_923044.2:n.620A>G
NM_001206524.2:c.416A>G	NP_001193453.1:p.Lys139Arg
NM_001206542.2:c.416A>G	NP_001193471.1:p.Lys139Arg
NM_001230.5:c.416A>G	NP_001221.2:p.Lys139Arg
NM_001306083.2:c.416A>G	NP_001293012.1:p.Lys139Arg
NM_032974.5:c.416A>G	NP_116756.2:p.Lys139Arg
NM_032977.4:c.416A>G MANE Select	NP_116759.2:p.Lys139Arg
NM_032976.4:c.416A>G	NP_116758.1:p.Lys139Arg