Canonical Allele Identifier: CA350286539

Gene: CASP10

Linked Data

• MyVariant Identifiers: chr2:g.202072861A>C (hg19) ; chr2:g.201208138A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201208138A>C , CM000664.2:g.201208138A>C	GRCh38
NC_000002.11:g.202072861A>C , CM000664.1:g.202072861A>C	GRCh37
NC_000002.10:g.201781106A>C	NCBI36
NG_007265.1:g.30007A>C , LRG_33:g.30007A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.722-932A>C	ENSP00000314599.7:n.722-932A>C
ENST00000346817.10:c.748A>C	ENSP00000237865.7:p.Ser250Arg
ENST00000438843.6:c.*334A>C	ENSP00000401914.1:n.*334A>C
ENST00000492363.6:c.785A>C	ENSP00000512459.1:p.Gln262Pro
ENST00000696199.1:c.721+4372A>C	ENSP00000512481.1:n.721+4372A>C
ENST00000286186.11:c.877A>C MANE Select	ENSP00000286186.6:p.Ser293Arg
ENST00000272879.9:c.877A>C	ENSP00000272879.5:p.Ser293Arg
ENST00000286186.10:c.877A>C	ENSP00000286186.6:p.Ser293Arg
ENST00000313728.11:c.722-932A>C	ENSP00000314599.7:n.722-932A>C
ENST00000346817.9:c.748A>C	ENSP00000237865.7:p.Ser250Arg
ENST00000360132.7:c.785A>C	ENSP00000353250.3:p.Gln262Pro
ENST00000438843.5:c.*334A>C	ENSP00000401914.1:n.*334A>C
ENST00000448480.1:c.748A>C	ENSP00000396835.1:p.Ser250Arg
ENST00000492363.5:n.785A>C
NM_001206524.1:c.722-932A>C	NP_001193453.1:n.722-932A>C
NM_001206542.1:c.748A>C	NP_001193471.1:p.Ser250Arg
NM_001230.4:c.748A>C	NP_001221.2:p.Ser250Arg
NM_032974.4:c.877A>C	NP_116756.2:p.Ser293Arg
NM_032976.3:c.785A>C	NP_116758.1:p.Gln262Pro
NM_032977.3:c.877A>C , LRG_33t1:c.877A>C	NP_116759.2:p.Ser293Arg
XM_005246907.2:c.874A>C	XP_005246964.1:p.Ser292Arg
XM_006712796.2:c.127A>C	XP_006712859.1:p.Ser43Arg
XM_011511990.1:c.782A>C	XP_011510292.1:p.Gln261Pro
XR_923043.1:n.1081A>C
XR_923044.1:n.989A>C
XM_006712796.3:c.127A>C	XP_006712859.1:p.Ser43Arg
XM_011511990.2:c.782A>C	XP_011510292.1:p.Gln261Pro
XR_923043.2:n.1081A>C
XR_923044.2:n.989A>C
NM_001206524.2:c.722-932A>C	NP_001193453.1:n.722-932A>C
NM_001206542.2:c.748A>C	NP_001193471.1:p.Ser250Arg
NM_001230.5:c.748A>C	NP_001221.2:p.Ser250Arg
NM_032974.5:c.877A>C	NP_116756.2:p.Ser293Arg
NM_032977.4:c.877A>C MANE Select	NP_116759.2:p.Ser293Arg
NM_032976.4:c.785A>C	NP_116758.1:p.Gln262Pro