Canonical Allele Identifier: CA343568877

Gene: NPHS2

Linked Data

• gnomAD v4: 1-179559716-T-A
• MyVariant Identifiers: chr1:g.179528851T>A (hg19) ; chr1:g.179559716T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179559716T>A , CM000663.2:g.179559716T>A	GRCh38
NC_000001.10:g.179528851T>A , CM000663.1:g.179528851T>A	GRCh37
NC_000001.9:g.177795474T>A	NCBI36
NG_007535.1:g.21234A>T , LRG_887:g.21234A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367615.9:c.497A>T MANE Select	ENSP00000356587.4:p.Asp166Val
ENST00000367615.8:c.497A>T	ENSP00000356587.4:p.Asp166Val
ENST00000367616.4:c.497A>T	ENSP00000356588.4:p.Asp166Val
NM_001297575.1:c.497A>T	NP_001284504.1:p.Asp166Val
NM_014625.3:c.497A>T , LRG_887t1:c.497A>T	NP_055440.1:p.Asp166Val
XM_005245483.2:c.320A>T	XP_005245540.1:p.Asp107Val
XM_006711529.2:c.497A>T	XP_006711592.1:p.Asp166Val
XM_005245483.3:c.320A>T	XP_005245540.1:p.Asp107Val
XM_017002298.1:c.424A>T	XP_016857787.1:p.Thr142Ser
XM_017002299.1:c.497A>T	XP_016857788.1:p.Asp166Val
NM_001297575.2:c.497A>T	NP_001284504.1:p.Asp166Val
NM_014625.4:c.497A>T MANE Select	NP_055440.1:p.Asp166Val