Canonical Allele Identifier: CA646095044

Gene: NPHS2

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179575915_179575916insA , CM000663.2:g.179575915_179575916insA	GRCh38
NC_000001.10:g.179545050_179545051insA , CM000663.1:g.179545050_179545051insA	GRCh37
NC_000001.9:g.177811673_177811674insA	NCBI36
NG_007535.1:g.5034_5035insT , LRG_887:g.5034_5035insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367615.9:c.-52_-51insT MANE Select	ENSP00000356587.4:n.-52_-51insT
ENST00000367615.8:c.-52_-51insT	ENSP00000356587.4:n.-52_-51insT
ENST00000367616.4:c.-52_-51insT	ENSP00000356588.4:n.-52_-51insT
NM_001297575.1:c.-52_-51insT	NP_001284504.1:n.-52_-51insT
NM_014625.3:c.-52_-51insT , LRG_887t1:c.-52_-51insT	NP_055440.1:n.-52_-51insT
XM_005245483.2:c.-52_-51insT	XP_005245540.1:n.-52_-51insT
XM_006711529.2:c.-52_-51insT	XP_006711592.1:n.-52_-51insT
XM_005245483.3:c.-52_-51insT	XP_005245540.1:n.-52_-51insT
XM_017002298.1:c.-52_-51insT	XP_016857787.1:n.-52_-51insT
XM_017002299.1:c.-52_-51insT	XP_016857788.1:n.-52_-51insT
NM_001297575.2:c.-52_-51insT	NP_001284504.1:n.-52_-51insT
NM_014625.4:c.-52_-51insT MANE Select	NP_055440.1:n.-52_-51insT