Canonical Allele Identifier: CA343568161

Gene: NPHS2

Linked Data

• MyVariant Identifiers: chr1:g.179526325A>T (hg19) ; chr1:g.179557190A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179557190A>T , CM000663.2:g.179557190A>T	GRCh38
NC_000001.10:g.179526325A>T , CM000663.1:g.179526325A>T	GRCh37
NC_000001.9:g.177792948A>T	NCBI36
NG_007535.1:g.23760T>A , LRG_887:g.23760T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367615.9:c.575T>A MANE Select	ENSP00000356587.4:p.Ile192Asn
ENST00000367615.8:c.575T>A	ENSP00000356587.4:p.Ile192Asn
ENST00000367616.4:c.534+2489T>A	ENSP00000356588.4:n.534+2489T>A
NM_001297575.1:c.534+2489T>A	NP_001284504.1:n.534+2489T>A
NM_014625.3:c.575T>A , LRG_887t1:c.575T>A	NP_055440.1:p.Ile192Asn
XM_005245483.2:c.398T>A	XP_005245540.1:p.Ile133Asn
XM_006711529.2:c.575T>A	XP_006711592.1:p.Ile192Asn
XM_005245483.3:c.398T>A	XP_005245540.1:p.Ile133Asn
XM_017002298.1:c.461+2489T>A	XP_016857787.1:n.461+2489T>A
XM_017002299.1:c.534+2489T>A	XP_016857788.1:n.534+2489T>A
NM_001297575.2:c.534+2489T>A	NP_001284504.1:n.534+2489T>A
NM_014625.4:c.575T>A MANE Select	NP_055440.1:p.Ile192Asn