Canonical Allele Identifier: CA1739083522
Gene: CPED1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.121263724T= , CM000669.2:g.121263724T= GRCh38
NC_000007.13:g.120903778T= , CM000669.1:g.120903778T= GRCh37
NC_000007.12:g.120691014T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000310396.10:c.2311-2503T= MANE Select ENSP00000309772.5:n.2311-2503T=
ENST00000310396.9:c.2311-2503T= ENSP00000309772.5:n.2311-2503T=
NM_024913.4:c.2311-2503T= NP_079189.4:n.2311-2503T=
XM_011516583.1:c.2311-2503T= XP_011514885.1:n.2311-2503T=
XR_927916.1:n.48+2937A=
XM_024446941.1:c.1798-2503T= XP_024302709.1:n.1798-2503T=
NM_024913.5:c.2311-2503T= MANE Select NP_079189.4:n.2311-2503T=
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