Canonical Allele Identifier: CA1106552893

Gene: CPED1

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.121107254T>A , CM000669.2:g.121107254T>A	GRCh38
NC_000007.13:g.120747308T>A , CM000669.1:g.120747308T>A	GRCh37
NC_000007.12:g.120534544T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310396.10:c.918+7160T>A MANE Select	ENSP00000309772.5:n.918+7160T>A
ENST00000310396.9:c.918+7160T>A	ENSP00000309772.5:n.918+7160T>A
ENST00000423795.5:c.258+7160T>A	ENSP00000415573.1:n.258+7160T>A
ENST00000428526.5:c.918+7160T>A	ENSP00000398082.1:n.918+7160T>A
ENST00000443817.1:c.258+7160T>A	ENSP00000391952.1:n.258+7160T>A
ENST00000450913.6:c.918+7160T>A	ENSP00000406122.2:n.918+7160T>A
NM_001105533.1:c.918+7160T>A	NP_001099003.1:n.918+7160T>A
NM_024913.4:c.918+7160T>A	NP_079189.4:n.918+7160T>A
XM_011516583.1:c.918+7160T>A	XP_011514885.1:n.918+7160T>A
XM_017012649.2:c.918+7160T>A	XP_016868138.1:n.918+7160T>A
XM_024446941.1:c.405+7160T>A	XP_024302709.1:n.405+7160T>A
NM_024913.5:c.918+7160T>A MANE Select	NP_079189.4:n.918+7160T>A