Canonical Allele Identifier: CA2649317014

Gene: NPHS2

Linked Data

• gnomAD v4: 1-179575751-GCGCCCGCGGCCTCCGCCGCTCCTCTCGGCCTTTGCCCTCTTGTTCTCCTTGTGCGGAGTCCTGCCGCCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179575761_179575829del , CM000663.2:g.179575761_179575829del	GRCh38
NC_000001.10:g.179544896_179544964del , CM000663.1:g.179544896_179544964del	GRCh37
NC_000001.9:g.177811519_177811587del	NCBI36
NG_007535.1:g.5130_5198del , LRG_887:g.5130_5198del

Transcript Alleles

HGVS	Amino-acid change
ENST00000367615.9:c.45_113del MANE Select	ENSP00000356587.4:p.Gly16_Arg38del
ENST00000367615.8:c.45_113del	ENSP00000356587.4:p.Gly16_Arg38del
ENST00000367616.4:c.45_113del	ENSP00000356588.4:p.Gly16_Arg38del
NM_001297575.1:c.45_113del	NP_001284504.1:p.Gly16_Arg38del
NM_014625.3:c.45_113del , LRG_887t1:c.45_113del	NP_055440.1:p.Gly16_Arg38del
XM_005245483.2:c.45_113del	XP_005245540.1:p.Gly16_Arg38del
XM_006711529.2:c.45_113del	XP_006711592.1:p.Gly16_Arg38del
XM_005245483.3:c.45_113del	XP_005245540.1:p.Gly16_Arg38del
XM_017002298.1:c.45_113del	XP_016857787.1:p.Gly16_Arg38del
XM_017002299.1:c.45_113del	XP_016857788.1:p.Gly16_Arg38del
NM_001297575.2:c.45_113del	NP_001284504.1:p.Gly16_Arg38del
NM_014625.4:c.45_113del MANE Select	NP_055440.1:p.Gly16_Arg38del