Canonical Allele Identifier: CA422026200

Gene: NPHS2

Linked Data

• MyVariant Identifiers: chr1:g.179530443A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179561308A>T , CM000663.2:g.179561308A>T	GRCh38
NC_000001.10:g.179530443A>T , CM000663.1:g.179530443A>T	GRCh37
NC_000001.9:g.177797066A>T	NCBI36
NG_007535.1:g.19642T>A , LRG_887:g.19642T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367615.9:c.432T>A MANE Select	ENSP00000356587.4:p.Pro144=
ENST00000367615.8:c.432T>A	ENSP00000356587.4:p.Pro144=
ENST00000367616.4:c.432T>A	ENSP00000356588.4:p.Pro144=
NM_001297575.1:c.432T>A	NP_001284504.1:p.Pro144=
NM_014625.3:c.432T>A , LRG_887t1:c.432T>A	NP_055440.1:p.Pro144=
XM_005245483.2:c.275-1547T>A	XP_005245540.1:n.275-1547T>A
XM_006711529.2:c.432T>A	XP_006711592.1:p.Pro144=
XM_005245483.3:c.275-1547T>A	XP_005245540.1:n.275-1547T>A
XM_017002298.1:c.379-1547T>A	XP_016857787.1:n.379-1547T>A
XM_017002299.1:c.432T>A	XP_016857788.1:p.Pro144=
NM_001297575.2:c.432T>A	NP_001284504.1:p.Pro144=
NM_014625.4:c.432T>A MANE Select	NP_055440.1:p.Pro144=