Canonical Allele Identifier: CA832405568

Gene: CPED1

Linked Data

• dbSNP Id: rs1260584187
• MyVariant Identifiers: chr7:g.120903864A>C (hg19) ; chr7:g.121263810A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.121263810A>C , CM000669.2:g.121263810A>C	GRCh38
NC_000007.13:g.120903864A>C , CM000669.1:g.120903864A>C	GRCh37
NC_000007.12:g.120691100A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000310396.10:c.2311-2417A>C MANE Select	ENSP00000309772.5:n.2311-2417A>C
ENST00000310396.9:c.2311-2417A>C	ENSP00000309772.5:n.2311-2417A>C
NM_024913.4:c.2311-2417A>C	NP_079189.4:n.2311-2417A>C
XM_011516583.1:c.2311-2417A>C	XP_011514885.1:n.2311-2417A>C
XR_927916.1:n.48+2851T>G
XM_024446941.1:c.1798-2417A>C	XP_024302709.1:n.1798-2417A>C
NM_024913.5:c.2311-2417A>C MANE Select	NP_079189.4:n.2311-2417A>C