Canonical Allele Identifier: CA1739011825

Gene: CPED1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.121102926C= , CM000669.2:g.121102926C=	GRCh38
NC_000007.13:g.120742980C= , CM000669.1:g.120742980C=	GRCh37
NC_000007.12:g.120530216C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_024913.5:c.918+2832C= MANE Select	NP_079189.4:n.918+2832C=
ENST00000310396.10:c.918+2832C= MANE Select	ENSP00000309772.5:n.918+2832C=
NM_001105533.1:c.918+2832C=	NP_001099003.1:n.918+2832C=
NM_024913.4:c.918+2832C=	NP_079189.4:n.918+2832C=
ENST00000310396.9:c.918+2832C=	ENSP00000309772.5:n.918+2832C=
ENST00000423795.5:c.258+2832C=	ENSP00000415573.1:n.258+2832C=
ENST00000428526.5:c.918+2832C=	ENSP00000398082.1:n.918+2832C=
ENST00000443817.1:c.258+2832C=	ENSP00000391952.1:n.258+2832C=
ENST00000450913.6:c.918+2832C=	ENSP00000406122.2:n.918+2832C=
XM_011516583.1:c.918+2832C=	XP_011514885.1:n.918+2832C=
XM_017012649.2:c.918+2832C=	XP_016868138.1:n.918+2832C=
XM_024446941.1:c.405+2832C=	XP_024302709.1:n.405+2832C=