Canonical Allele Identifier: CA1210319062

Gene: NPHS2

Linked Data

• dbSNP Id: rs1572276804

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179556598G>T , CM000663.2:g.179556598G>T	GRCh38
NC_000001.10:g.179525733G>T , CM000663.1:g.179525733G>T	GRCh37
NC_000001.9:g.177792356G>T	NCBI36
NG_007535.1:g.24352C>A , LRG_887:g.24352C>A
NG_033075.1:g.195879G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367615.9:c.738+429C>A MANE Select	ENSP00000356587.4:n.738+429C>A
ENST00000367615.8:c.738+429C>A	ENSP00000356587.4:n.738+429C>A
ENST00000367616.4:c.535-2067C>A	ENSP00000356588.4:n.535-2067C>A
NM_001297575.1:c.535-2067C>A	NP_001284504.1:n.535-2067C>A
NM_014625.3:c.738+429C>A , LRG_887t1:c.738+429C>A	NP_055440.1:n.738+429C>A
XM_005245483.2:c.561+429C>A	XP_005245540.1:n.561+429C>A
XM_006711529.2:c.738+429C>A	XP_006711592.1:n.738+429C>A
XM_005245483.3:c.561+429C>A	XP_005245540.1:n.561+429C>A
XM_017002298.1:c.461+3081C>A	XP_016857787.1:n.461+3081C>A
XM_017002299.1:c.534+3081C>A	XP_016857788.1:n.534+3081C>A
NM_001297575.2:c.535-2067C>A	NP_001284504.1:n.535-2067C>A
NM_014625.4:c.738+429C>A MANE Select	NP_055440.1:n.738+429C>A