Canonical Allele Identifier: CA1320967342
Gene: CASP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201209374_201209375delinsCG , CM000664.2:g.201209374_201209375delinsCG GRCh38
NC_000002.11:g.202074097_202074098delinsCG , CM000664.1:g.202074097_202074098delinsCG GRCh37
NC_000002.10:g.201782342_201782343delinsCG NCBI36
NG_007265.1:g.31243_31244delinsCG , LRG_33:g.31243_31244delinsCG

Transcript Alleles

HGVS Amino-acid change
ENST00000313728.12:c.1026_1027delinsCG ENSP00000314599.7:p.Ser342=
ENST00000346817.10:c.1098_1099delinsCG ENSP00000237865.7:p.Ser366=
ENST00000438843.6:c.*684_*685delinsCG ENSP00000401914.1:n.*684_*685delinsCG
ENST00000492363.6:c.*313_*314delinsCG ENSP00000512459.1:n.*313_*314delinsCG
ENST00000696199.1:c.721+5608_721+5609delinsCG ENSP00000512481.1:n.721+5608_721+5609deli...
ENST00000286186.11:c.1227_1228delinsCG MANE Select ENSP00000286186.6:p.Ser409=
ENST00000272879.9:c.1227_1228delinsCG ENSP00000272879.5:p.Ser409=
ENST00000286186.10:c.1227_1228delinsCG ENSP00000286186.6:p.Ser409=
ENST00000313728.11:c.1026_1027delinsCG ENSP00000314599.7:p.Ser342=
ENST00000346817.9:c.1098_1099delinsCG ENSP00000237865.7:p.Ser366=
ENST00000360132.7:c.*313_*314delinsCG ENSP00000353250.3:n.*313_*314delinsCG
ENST00000448480.1:c.1098_1099delinsCG ENSP00000396835.1:p.Ser366=
ENST00000492363.5:n.1135_1136delinsCG
NM_001206524.1:c.1026_1027delinsCG NP_001193453.1:p.Ser342=
NM_001206542.1:c.1098_1099delinsCG NP_001193471.1:p.Ser366=
NM_001230.4:c.1098_1099delinsCG NP_001221.2:p.Ser366=
NM_032974.4:c.1227_1228delinsCG NP_116756.2:p.Ser409=
NM_032976.3:c.*313_*314delinsCG NP_116758.1:n.*313_*314delinsCG
NM_032977.3:c.1227_1228delinsCG , LRG_33t1:c.1227_1228delinsCG NP_116759.2:p.Ser409=
XM_005246907.2:c.1224_1225delinsCG XP_005246964.1:p.Ser408=
XM_006712796.2:c.477_478delinsCG XP_006712859.1:p.Ser159=
XM_006712796.3:c.477_478delinsCG XP_006712859.1:p.Ser159=
NM_001206524.2:c.1026_1027delinsCG NP_001193453.1:p.Ser342=
NM_001206542.2:c.1098_1099delinsCG NP_001193471.1:p.Ser366=
NM_001230.5:c.1098_1099delinsCG NP_001221.2:p.Ser366=
NM_032974.5:c.1227_1228delinsCG NP_116756.2:p.Ser409=
NM_032977.4:c.1227_1228delinsCG MANE Select NP_116759.2:p.Ser409=
NM_032976.4:c.*313_*314delinsCG NP_116758.1:n.*313_*314delinsCG