Canonical Allele Identifier: CA1210319049

Gene: NPHS2

Linked Data

• dbSNP Id: rs1673938316

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179556560G>A , CM000663.2:g.179556560G>A	GRCh38
NC_000001.10:g.179525695G>A , CM000663.1:g.179525695G>A	GRCh37
NC_000001.9:g.177792318G>A	NCBI36
NG_007535.1:g.24390C>T , LRG_887:g.24390C>T
NG_033075.1:g.195841G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367615.9:c.738+467C>T MANE Select	ENSP00000356587.4:n.738+467C>T
ENST00000367615.8:c.738+467C>T	ENSP00000356587.4:n.738+467C>T
ENST00000367616.4:c.535-2029C>T	ENSP00000356588.4:n.535-2029C>T
NM_001297575.1:c.535-2029C>T	NP_001284504.1:n.535-2029C>T
NM_014625.3:c.738+467C>T , LRG_887t1:c.738+467C>T	NP_055440.1:n.738+467C>T
XM_005245483.2:c.561+467C>T	XP_005245540.1:n.561+467C>T
XM_006711529.2:c.738+467C>T	XP_006711592.1:n.738+467C>T
XM_005245483.3:c.561+467C>T	XP_005245540.1:n.561+467C>T
XM_017002298.1:c.461+3119C>T	XP_016857787.1:n.461+3119C>T
XM_017002299.1:c.534+3119C>T	XP_016857788.1:n.534+3119C>T
NM_001297575.2:c.535-2029C>T	NP_001284504.1:n.535-2029C>T
NM_014625.4:c.738+467C>T MANE Select	NP_055440.1:n.738+467C>T