Canonical Allele Identifier: CA350291103

Gene: CASP10

Linked Data

• MyVariant Identifiers: chr2:g.202073950A>C (hg19) ; chr2:g.201209227A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201209227A>C , CM000664.2:g.201209227A>C	GRCh38
NC_000002.11:g.202073950A>C , CM000664.1:g.202073950A>C	GRCh37
NC_000002.10:g.201782195A>C	NCBI36
NG_007265.1:g.31096A>C , LRG_33:g.31096A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.879A>C	ENSP00000314599.7:p.Arg293Ser
ENST00000346817.10:c.951A>C	ENSP00000237865.7:p.Arg317Ser
ENST00000438843.6:c.*537A>C	ENSP00000401914.1:n.*537A>C
ENST00000492363.6:c.*166A>C	ENSP00000512459.1:n.*166A>C
ENST00000696199.1:c.721+5461A>C	ENSP00000512481.1:n.721+5461A>C
ENST00000286186.11:c.1080A>C MANE Select	ENSP00000286186.6:p.Arg360Ser
ENST00000272879.9:c.1080A>C	ENSP00000272879.5:p.Arg360Ser
ENST00000286186.10:c.1080A>C	ENSP00000286186.6:p.Arg360Ser
ENST00000313728.11:c.879A>C	ENSP00000314599.7:p.Arg293Ser
ENST00000346817.9:c.951A>C	ENSP00000237865.7:p.Arg317Ser
ENST00000360132.7:c.*166A>C	ENSP00000353250.3:n.*166A>C
ENST00000448480.1:c.951A>C	ENSP00000396835.1:p.Arg317Ser
ENST00000492363.5:n.988A>C
NM_001206524.1:c.879A>C	NP_001193453.1:p.Arg293Ser
NM_001206542.1:c.951A>C	NP_001193471.1:p.Arg317Ser
NM_001230.4:c.951A>C	NP_001221.2:p.Arg317Ser
NM_032974.4:c.1080A>C	NP_116756.2:p.Arg360Ser
NM_032976.3:c.*166A>C	NP_116758.1:n.*166A>C
NM_032977.3:c.1080A>C , LRG_33t1:c.1080A>C	NP_116759.2:p.Arg360Ser
XM_005246907.2:c.1077A>C	XP_005246964.1:p.Arg359Ser
XM_006712796.2:c.330A>C	XP_006712859.1:p.Arg110Ser
XM_006712796.3:c.330A>C	XP_006712859.1:p.Arg110Ser
NM_001206524.2:c.879A>C	NP_001193453.1:p.Arg293Ser
NM_001206542.2:c.951A>C	NP_001193471.1:p.Arg317Ser
NM_001230.5:c.951A>C	NP_001221.2:p.Arg317Ser
NM_032974.5:c.1080A>C	NP_116756.2:p.Arg360Ser
NM_032977.4:c.1080A>C MANE Select	NP_116759.2:p.Arg360Ser
NM_032976.4:c.*166A>C	NP_116758.1:n.*166A>C