Canonical Allele Identifier: CA1739083481
Gene: CPED1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.121263679_121263685delinsTTTGTTG , CM000669.2:g.121263679_121263685delinsTTTGTTG GRCh38
NC_000007.13:g.120903733_120903739delinsTTTGTTG , CM000669.1:g.120903733_120903739delinsTTTGTTG GRCh37
NC_000007.12:g.120690969_120690975delinsTTTGTTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310396.10:c.2311-2548_2311-2542delinsTTTGTTG MANE Select ENSP00000309772.5:n.2311-2548_2311-2542delinsTTTGTTG
ENST00000310396.9:c.2311-2548_2311-2542delinsTTTGTTG ENSP00000309772.5:n.2311-2548_2311-2542delinsTTTGTTG
NM_024913.4:c.2311-2548_2311-2542delinsTTTGTTG NP_079189.4:n.2311-2548_2311-2542delinsTTTGTTG
XM_011516583.1:c.2311-2548_2311-2542delinsTTTGTTG XP_011514885.1:n.2311-2548_2311-2542delinsTTTGTTG
XR_927916.1:n.48+2976_48+2982delinsCAACAAA
XM_024446941.1:c.1798-2548_1798-2542delinsTTTGTTG XP_024302709.1:n.1798-2548_1798-2542delinsTTTGTTG
NM_024913.5:c.2311-2548_2311-2542delinsTTTGTTG MANE Select NP_079189.4:n.2311-2548_2311-2542delinsTTTGTTG
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