Canonical Allele Identifier: CA2053173
Gene: CASP10 HGNC NCBI

Linked Data

dbSNP Id: rs762087406

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201209201G>A , CM000664.2:g.201209201G>A GRCh38
NC_000002.11:g.202073924G>A , CM000664.1:g.202073924G>A GRCh37
NC_000002.10:g.201782169G>A NCBI36
NG_007265.1:g.31070G>A , LRG_33:g.31070G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000313728.12:c.853G>A ENSP00000314599.7:p.Val285Met
ENST00000346817.10:c.925G>A ENSP00000237865.7:p.Val309Met
ENST00000438843.6:c.*511G>A ENSP00000401914.1:n.*511G>A
ENST00000492363.6:c.*140G>A ENSP00000512459.1:n.*140G>A
ENST00000696199.1:c.721+5435G>A ENSP00000512481.1:n.721+5435G>A
ENST00000286186.11:c.1054G>A MANE Select ENSP00000286186.6:p.Val352Met
ENST00000272879.9:c.1054G>A ENSP00000272879.5:p.Val352Met
ENST00000286186.10:c.1054G>A ENSP00000286186.6:p.Val352Met
ENST00000313728.11:c.853G>A ENSP00000314599.7:p.Val285Met
ENST00000346817.9:c.925G>A ENSP00000237865.7:p.Val309Met
ENST00000360132.7:c.*140G>A ENSP00000353250.3:n.*140G>A
ENST00000448480.1:c.925G>A ENSP00000396835.1:p.Val309Met
ENST00000492363.5:n.962G>A
NM_001206524.1:c.853G>A NP_001193453.1:p.Val285Met
NM_001206542.1:c.925G>A NP_001193471.1:p.Val309Met
NM_001230.4:c.925G>A NP_001221.2:p.Val309Met
NM_032974.4:c.1054G>A NP_116756.2:p.Val352Met
NM_032976.3:c.*140G>A NP_116758.1:n.*140G>A
NM_032977.3:c.1054G>A , LRG_33t1:c.1054G>A NP_116759.2:p.Val352Met
XM_005246907.2:c.1051G>A XP_005246964.1:p.Val351Met
XM_006712796.2:c.304G>A XP_006712859.1:p.Val102Met
XM_006712796.3:c.304G>A XP_006712859.1:p.Val102Met
NM_001206524.2:c.853G>A NP_001193453.1:p.Val285Met
NM_001206542.2:c.925G>A NP_001193471.1:p.Val309Met
NM_001230.5:c.925G>A NP_001221.2:p.Val309Met
NM_032974.5:c.1054G>A NP_116756.2:p.Val352Met
NM_032977.4:c.1054G>A MANE Select NP_116759.2:p.Val352Met
NM_032976.4:c.*140G>A NP_116758.1:n.*140G>A