Canonical Allele Identifier: CA1739083468
Gene: CPED1 HGNC NCBI

Linked Data

dbSNP Id: rs1259889483
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.121263671C>T , CM000669.2:g.121263671C>T GRCh38
NC_000007.13:g.120903725C>T , CM000669.1:g.120903725C>T GRCh37
NC_000007.12:g.120690961C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000310396.10:c.2311-2556C>T MANE Select ENSP00000309772.5:n.2311-2556C>T
ENST00000310396.9:c.2311-2556C>T ENSP00000309772.5:n.2311-2556C>T
NM_024913.4:c.2311-2556C>T NP_079189.4:n.2311-2556C>T
XM_011516583.1:c.2311-2556C>T XP_011514885.1:n.2311-2556C>T
XR_927916.1:n.48+2990G>A
XM_024446941.1:c.1798-2556C>T XP_024302709.1:n.1798-2556C>T
NM_024913.5:c.2311-2556C>T MANE Select NP_079189.4:n.2311-2556C>T
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