Canonical Allele Identifier: CA350286580

Gene: CASP10

Linked Data

• MyVariant Identifiers: chr2:g.202072865T>C (hg19) ; chr2:g.201208142T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201208142T>C , CM000664.2:g.201208142T>C	GRCh38
NC_000002.11:g.202072865T>C , CM000664.1:g.202072865T>C	GRCh37
NC_000002.10:g.201781110T>C	NCBI36
NG_007265.1:g.30011T>C , LRG_33:g.30011T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.722-928T>C	ENSP00000314599.7:n.722-928T>C
ENST00000346817.10:c.752T>C	ENSP00000237865.7:p.Phe251Ser
ENST00000438843.6:c.*338T>C	ENSP00000401914.1:n.*338T>C
ENST00000492363.6:c.789T>C	ENSP00000512459.1:p.Leu263=
ENST00000696199.1:c.721+4376T>C	ENSP00000512481.1:n.721+4376T>C
ENST00000286186.11:c.881T>C MANE Select	ENSP00000286186.6:p.Phe294Ser
ENST00000272879.9:c.881T>C	ENSP00000272879.5:p.Phe294Ser
ENST00000286186.10:c.881T>C	ENSP00000286186.6:p.Phe294Ser
ENST00000313728.11:c.722-928T>C	ENSP00000314599.7:n.722-928T>C
ENST00000346817.9:c.752T>C	ENSP00000237865.7:p.Phe251Ser
ENST00000360132.7:c.789T>C	ENSP00000353250.3:p.Leu263=
ENST00000438843.5:c.*338T>C	ENSP00000401914.1:n.*338T>C
ENST00000448480.1:c.752T>C	ENSP00000396835.1:p.Phe251Ser
ENST00000492363.5:n.789T>C
NM_001206524.1:c.722-928T>C	NP_001193453.1:n.722-928T>C
NM_001206542.1:c.752T>C	NP_001193471.1:p.Phe251Ser
NM_001230.4:c.752T>C	NP_001221.2:p.Phe251Ser
NM_032974.4:c.881T>C	NP_116756.2:p.Phe294Ser
NM_032976.3:c.789T>C	NP_116758.1:p.Leu263=
NM_032977.3:c.881T>C , LRG_33t1:c.881T>C	NP_116759.2:p.Phe294Ser
XM_005246907.2:c.878T>C	XP_005246964.1:p.Phe293Ser
XM_006712796.2:c.131T>C	XP_006712859.1:p.Phe44Ser
XM_011511990.1:c.786T>C	XP_011510292.1:p.Leu262=
XR_923043.1:n.1085T>C
XR_923044.1:n.993T>C
XM_006712796.3:c.131T>C	XP_006712859.1:p.Phe44Ser
XM_011511990.2:c.786T>C	XP_011510292.1:p.Leu262=
XR_923043.2:n.1085T>C
XR_923044.2:n.993T>C
NM_001206524.2:c.722-928T>C	NP_001193453.1:n.722-928T>C
NM_001206542.2:c.752T>C	NP_001193471.1:p.Phe251Ser
NM_001230.5:c.752T>C	NP_001221.2:p.Phe251Ser
NM_032974.5:c.881T>C	NP_116756.2:p.Phe294Ser
NM_032977.4:c.881T>C MANE Select	NP_116759.2:p.Phe294Ser
NM_032976.4:c.789T>C	NP_116758.1:p.Leu263=