Canonical Allele Identifier: CA1739083499
Gene: CPED1 HGNC NCBI

Linked Data

dbSNP Id: rs1792063239

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.121263693dup , CM000669.2:g.121263693dup GRCh38
NC_000007.13:g.120903747dup , CM000669.1:g.120903747dup GRCh37
NC_000007.12:g.120690983dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000310396.10:c.2311-2534dup MANE Select ENSP00000309772.5:n.2311-2534dup
ENST00000310396.9:c.2311-2534dup ENSP00000309772.5:n.2311-2534dup
NM_024913.4:c.2311-2534dup NP_079189.4:n.2311-2534dup
XM_011516583.1:c.2311-2534dup XP_011514885.1:n.2311-2534dup
XR_927916.1:n.48+2972dup
XM_024446941.1:c.1798-2534dup XP_024302709.1:n.1798-2534dup
NM_024913.5:c.2311-2534dup MANE Select NP_079189.4:n.2311-2534dup