Canonical Allele Identifier: CA1140978631

Gene: NPHS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179575593T= , CM000663.2:g.179575593T=	GRCh38
NC_000001.10:g.179544728T= , CM000663.1:g.179544728T=	GRCh37
NC_000001.9:g.177811351T=	NCBI36
NG_007535.1:g.5357A= , LRG_887:g.5357A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367615.9:c.272A= MANE Select	ENSP00000356587.4:p.Glu91=
ENST00000367615.8:c.272A=	ENSP00000356587.4:p.Glu91=
ENST00000367616.4:c.272A=	ENSP00000356588.4:p.Glu91=
NM_001297575.1:c.272A=	NP_001284504.1:p.Glu91=
NM_014625.3:c.272A= , LRG_887t1:c.272A=	NP_055440.1:p.Glu91=
XM_005245483.2:c.272A=	XP_005245540.1:p.Glu91=
XM_006711529.2:c.272A=	XP_006711592.1:p.Glu91=
XM_005245483.3:c.272A=	XP_005245540.1:p.Glu91=
XM_017002298.1:c.272A=	XP_016857787.1:p.Glu91=
XM_017002299.1:c.272A=	XP_016857788.1:p.Glu91=
NM_001297575.2:c.272A=	NP_001284504.1:p.Glu91=
NM_014625.4:c.272A= MANE Select	NP_055440.1:p.Glu91=