Canonical Allele Identifier: CA1739016339

Gene: CPED1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.121136045G= , CM000669.2:g.121136045G=	GRCh38
NC_000007.13:g.120776099G= , CM000669.1:g.120776099G=	GRCh37
NC_000007.12:g.120563335G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310396.10:c.1654G= MANE Select	ENSP00000309772.5:p.Val552=
ENST00000310396.9:c.1654G=	ENSP00000309772.5:p.Val552=
ENST00000423795.5:c.994G=	ENSP00000415573.1:p.Val332=
ENST00000443817.1:c.994G=	ENSP00000391952.1:p.Val332=
ENST00000450913.6:c.1654G=	ENSP00000406122.2:p.Val552=
NM_001105533.1:c.1654G=	NP_001099003.1:p.Val552=
NM_024913.4:c.1654G=	NP_079189.4:p.Val552=
XM_011516583.1:c.1654G=	XP_011514885.1:p.Val552=
XM_017012649.2:c.1654G=	XP_016868138.1:p.Val552=
XM_024446941.1:c.1141G=	XP_024302709.1:p.Val381=
NM_024913.5:c.1654G= MANE Select	NP_079189.4:p.Val552=