Canonical Allele Identifier: CA343554024

Gene: NPHS2

Linked Data

• gnomAD v4: 1-179575779-G-T
• MyVariant Identifiers: chr1:g.179544914G>T (hg19) ; chr1:g.179575779G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179575779G>T , CM000663.2:g.179575779G>T	GRCh38
NC_000001.10:g.179544914G>T , CM000663.1:g.179544914G>T	GRCh37
NC_000001.9:g.177811537G>T	NCBI36
NG_007535.1:g.5171C>A , LRG_887:g.5171C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367615.9:c.86C>A MANE Select	ENSP00000356587.4:p.Ala29Asp
ENST00000367615.8:c.86C>A	ENSP00000356587.4:p.Ala29Asp
ENST00000367616.4:c.86C>A	ENSP00000356588.4:p.Ala29Asp
NM_001297575.1:c.86C>A	NP_001284504.1:p.Ala29Asp
NM_014625.3:c.86C>A , LRG_887t1:c.86C>A	NP_055440.1:p.Ala29Asp
XM_005245483.2:c.86C>A	XP_005245540.1:p.Ala29Asp
XM_006711529.2:c.86C>A	XP_006711592.1:p.Ala29Asp
XM_005245483.3:c.86C>A	XP_005245540.1:p.Ala29Asp
XM_017002298.1:c.86C>A	XP_016857787.1:p.Ala29Asp
XM_017002299.1:c.86C>A	XP_016857788.1:p.Ala29Asp
NM_001297575.2:c.86C>A	NP_001284504.1:p.Ala29Asp
NM_014625.4:c.86C>A MANE Select	NP_055440.1:p.Ala29Asp