Canonical Allele Identifier: CA66363007

Gene: SGPP2

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.222488727A>C , CM000664.2:g.222488727A>C	GRCh38
NC_000002.11:g.223353446A>C , CM000664.1:g.223353446A>C	GRCh37
NC_000002.10:g.223061690A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321276.8:c.378+14001A>C MANE Select	ENSP00000315137.7:n.378+14001A>C
ENST00000321276.7:c.378+14001A>C	ENSP00000315137.7:n.378+14001A>C
NM_152386.2:c.378+14001A>C	NP_689599.2:n.378+14001A>C
XM_005246297.2:c.-7+14001A>C	XP_005246354.1:n.-7+14001A>C
NM_001320833.1:c.-7+14001A>C	NP_001307762.1:n.-7+14001A>C
NM_001320834.1:c.-7+14001A>C	NP_001307763.1:n.-7+14001A>C
NM_152386.3:c.378+14001A>C	NP_689599.2:n.378+14001A>C
XM_017003355.1:c.-7+14001A>C	XP_016858844.1:n.-7+14001A>C
NM_152386.4:c.378+14001A>C MANE Select	NP_689599.2:n.378+14001A>C
NM_001320833.2:c.-7+14001A>C	NP_001307762.1:n.-7+14001A>C
NM_001320834.2:c.-7+14001A>C	NP_001307763.1:n.-7+14001A>C