Canonical Allele Identifier: CA1210326722

Gene: NPHS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179575762_179575763delinsCT , CM000663.2:g.179575762_179575763delinsCT	GRCh38
NC_000001.10:g.179544897_179544898delinsCT , CM000663.1:g.179544897_179544898delinsCT	GRCh37
NC_000001.9:g.177811520_177811521delinsCT	NCBI36
NG_007535.1:g.5187_5188delinsAG , LRG_887:g.5187_5188delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000367615.9:c.102_103delinsAG MANE Select	ENSP00000356587.4:p.Gly34=
ENST00000367615.8:c.102_103delinsAG	ENSP00000356587.4:p.Gly34=
ENST00000367616.4:c.102_103delinsAG	ENSP00000356588.4:p.Gly34=
NM_001297575.1:c.102_103delinsAG	NP_001284504.1:p.Gly34=
NM_014625.3:c.102_103delinsAG , LRG_887t1:c.102_103delinsAG	NP_055440.1:p.Gly34=
XM_005245483.2:c.102_103delinsAG	XP_005245540.1:p.Gly34=
XM_006711529.2:c.102_103delinsAG	XP_006711592.1:p.Gly34=
XM_005245483.3:c.102_103delinsAG	XP_005245540.1:p.Gly34=
XM_017002298.1:c.102_103delinsAG	XP_016857787.1:p.Gly34=
XM_017002299.1:c.102_103delinsAG	XP_016857788.1:p.Gly34=
NM_001297575.2:c.102_103delinsAG	NP_001284504.1:p.Gly34=
NM_014625.4:c.102_103delinsAG MANE Select	NP_055440.1:p.Gly34=