Canonical Allele Identifier: CA343569080

Gene: NPHS2

Linked Data

• MyVariant Identifiers: chr1:g.179528891A>C (hg19) ; chr1:g.179559756A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179559756A>C , CM000663.2:g.179559756A>C	GRCh38
NC_000001.10:g.179528891A>C , CM000663.1:g.179528891A>C	GRCh37
NC_000001.9:g.177795514A>C	NCBI36
NG_007535.1:g.21194T>G , LRG_887:g.21194T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367615.9:c.457T>G MANE Select	ENSP00000356587.4:p.Phe153Val
ENST00000367615.8:c.457T>G	ENSP00000356587.4:p.Phe153Val
ENST00000367616.4:c.457T>G	ENSP00000356588.4:p.Phe153Val
NM_001297575.1:c.457T>G	NP_001284504.1:p.Phe153Val
NM_014625.3:c.457T>G , LRG_887t1:c.457T>G	NP_055440.1:p.Phe153Val
XM_005245483.2:c.280T>G	XP_005245540.1:p.Phe94Val
XM_006711529.2:c.457T>G	XP_006711592.1:p.Phe153Val
XM_005245483.3:c.280T>G	XP_005245540.1:p.Phe94Val
XM_017002298.1:c.384T>G	XP_016857787.1:p.Phe128Leu
XM_017002299.1:c.457T>G	XP_016857788.1:p.Phe153Val
NM_001297575.2:c.457T>G	NP_001284504.1:p.Phe153Val
NM_014625.4:c.457T>G MANE Select	NP_055440.1:p.Phe153Val