Canonical Allele Identifier: CA343567609

Gene: NPHS2

Linked Data

• dbSNP Id: rs61747728
• MyVariant Identifiers: chr1:g.179526214C>G (hg19) ; chr1:g.179557079C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179557079C>G , CM000663.2:g.179557079C>G	GRCh38
NC_000001.10:g.179526214C>G , CM000663.1:g.179526214C>G	GRCh37
NC_000001.9:g.177792837C>G	NCBI36
NG_007535.1:g.23871G>C , LRG_887:g.23871G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367615.9:c.686G>C MANE Select	ENSP00000356587.4:p.Arg229Pro
ENST00000367615.8:c.686G>C	ENSP00000356587.4:p.Arg229Pro
ENST00000367616.4:c.535-2548G>C	ENSP00000356588.4:n.535-2548G>C
NM_001297575.1:c.535-2548G>C	NP_001284504.1:n.535-2548G>C
NM_014625.3:c.686G>C , LRG_887t1:c.686G>C	NP_055440.1:p.Arg229Pro
XM_005245483.2:c.509G>C	XP_005245540.1:p.Arg170Pro
XM_006711529.2:c.686G>C	XP_006711592.1:p.Arg229Pro
XM_005245483.3:c.509G>C	XP_005245540.1:p.Arg170Pro
XM_017002298.1:c.461+2600G>C	XP_016857787.1:n.461+2600G>C
XM_017002299.1:c.534+2600G>C	XP_016857788.1:n.534+2600G>C
NM_001297575.2:c.535-2548G>C	NP_001284504.1:n.535-2548G>C
NM_014625.4:c.686G>C MANE Select	NP_055440.1:p.Arg229Pro