Canonical Allele Identifier: CA1937490543

Gene: CASP7

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113729393C= , CM000672.2:g.113729393C=	GRCh38
NC_000010.10:g.115489152C= , CM000672.1:g.115489152C=	GRCh37
NC_000010.9:g.115479142C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001227.5:c.765C= MANE Select	NP_001218.1:p.Asp255=
ENST00000369318.8:c.765C= MANE Select	ENSP00000358324.4:p.Asp255=
NM_001227.4:c.765C=	NP_001218.1:p.Asp255=
NM_001267056.1:c.765C=	NP_001253985.1:p.Asp255=
NM_001267056.2:c.765C=	NP_001253985.1:p.Asp255=
NM_001267057.1:c.1020C=	NP_001253986.1:p.Asp340=
NM_001267058.1:c.690C=	NP_001253987.1:p.Asp230=
NM_001267058.2:c.690C=	NP_001253987.1:p.Asp230=
NM_001320911.1:c.789C=	NP_001307840.1:p.Asp263=
NM_001320911.2:c.789C=	NP_001307840.1:p.Asp263=
NM_033338.5:c.864C=	NP_203124.1:p.Asp288=
NM_033338.6:c.864C=	NP_203124.1:p.Asp288=
NM_033339.4:c.765C=	NP_203125.1:p.Asp255=
NM_033339.5:c.765C=	NP_203125.1:p.Asp255=
NM_033340.3:c.731C=	NP_203126.1:p.Thr244=
NM_033340.4:c.731C=	NP_203126.1:p.Thr244=
ENST00000345633.8:c.765C=	ENSP00000298701.7:p.Asp255=
ENST00000369315.5:c.765C=	ENSP00000358321.1:p.Asp255=
ENST00000369318.7:c.765C=	ENSP00000358324.3:p.Asp255=
ENST00000369321.6:c.1020C=	ENSP00000358327.3:p.Asp340=
ENST00000369331.8:c.731C=	ENSP00000358337.3:p.Thr244=
ENST00000452490.3:c.690C=	ENSP00000398107.2:p.Asp230=
ENST00000487232.1:n.689C=
ENST00000614447.4:c.731C=	ENSP00000478285.1:p.Thr244=
ENST00000621345.4:c.765C=	ENSP00000480584.1:p.Asp255=
ENST00000621607.4:c.864C=	ENSP00000478999.1:p.Asp288=
ENST00000672138.1:c.762C=	ENSP00000500735.1:p.Asp254=
XM_006718017.2:c.807C=	XP_006718080.1:p.Asp269=
XM_006718017.3:c.807C=	XP_006718080.1:p.Asp269=
XM_006718018.1:c.789C=	XP_006718081.1:p.Asp263=
XM_011540259.1:c.864C=	XP_011538561.1:p.Asp288=
XM_011540260.1:c.666C=	XP_011538562.1:p.Asp222=
XM_017016763.1:c.822C=	XP_016872252.1:p.Asp274=
XM_017016764.1:c.789C=	XP_016872253.1:p.Asp263=