Canonical Allele Identifier: CA1739014012

Gene: CPED1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.121145010A= , CM000669.2:g.121145010A=	GRCh38
NC_000007.13:g.120785064A= , CM000669.1:g.120785064A=	GRCh37
NC_000007.12:g.120572300A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310396.10:c.2055+2869A= MANE Select	ENSP00000309772.5:n.2055+2869A=
ENST00000310396.9:c.2055+2869A=	ENSP00000309772.5:n.2055+2869A=
ENST00000423795.5:c.1395+2869A=	ENSP00000415573.1:n.1395+2869A=
ENST00000450913.6:c.2055+2869A=	ENSP00000406122.2:n.2055+2869A=
NM_001105533.1:c.2055+2869A=	NP_001099003.1:n.2055+2869A=
NM_024913.4:c.2055+2869A=	NP_079189.4:n.2055+2869A=
XM_011516583.1:c.2055+2869A=	XP_011514885.1:n.2055+2869A=
XM_017012649.2:c.2055+2869A=	XP_016868138.1:n.2055+2869A=
XM_024446941.1:c.1542+2869A=	XP_024302709.1:n.1542+2869A=
NM_024913.5:c.2055+2869A= MANE Select	NP_079189.4:n.2055+2869A=