Canonical Allele Identifier: CA1739083614
Gene: CPED1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.121263830A= , CM000669.2:g.121263830A= GRCh38
NC_000007.13:g.120903884A= , CM000669.1:g.120903884A= GRCh37
NC_000007.12:g.120691120A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000310396.10:c.2311-2397A= MANE Select ENSP00000309772.5:n.2311-2397A=
ENST00000310396.9:c.2311-2397A= ENSP00000309772.5:n.2311-2397A=
NM_024913.4:c.2311-2397A= NP_079189.4:n.2311-2397A=
XM_011516583.1:c.2311-2397A= XP_011514885.1:n.2311-2397A=
XR_927916.1:n.48+2831T=
XM_024446941.1:c.1798-2397A= XP_024302709.1:n.1798-2397A=
NM_024913.5:c.2311-2397A= MANE Select NP_079189.4:n.2311-2397A=
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