Canonical Allele Identifier: CA2580773968
Gene: CPED1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.121263761A>G , CM000669.2:g.121263761A>G GRCh38
NC_000007.13:g.120903815A>G , CM000669.1:g.120903815A>G GRCh37
NC_000007.12:g.120691051A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310396.10:c.2311-2466A>G MANE Select ENSP00000309772.5:n.2311-2466A>G
ENST00000310396.9:c.2311-2466A>G ENSP00000309772.5:n.2311-2466A>G
NM_024913.4:c.2311-2466A>G NP_079189.4:n.2311-2466A>G
XM_011516583.1:c.2311-2466A>G XP_011514885.1:n.2311-2466A>G
XR_927916.1:n.48+2900T>C
XM_024446941.1:c.1798-2466A>G XP_024302709.1:n.1798-2466A>G
NM_024913.5:c.2311-2466A>G MANE Select NP_079189.4:n.2311-2466A>G
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