Canonical Allele Identifier: CA1140886939

Gene: NPHS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179575591C= , CM000663.2:g.179575591C=	GRCh38
NC_000001.10:g.179544726C= , CM000663.1:g.179544726C=	GRCh37
NC_000001.9:g.177811349C=	NCBI36
NG_007535.1:g.5359G= , LRG_887:g.5359G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367615.9:c.274G= MANE Select	ENSP00000356587.4:p.Gly92=
ENST00000367615.8:c.274G=	ENSP00000356587.4:p.Gly92=
ENST00000367616.4:c.274G=	ENSP00000356588.4:p.Gly92=
NM_001297575.1:c.274G=	NP_001284504.1:p.Gly92=
NM_014625.3:c.274G= , LRG_887t1:c.274G=	NP_055440.1:p.Gly92=
XM_005245483.2:c.274G=	XP_005245540.1:p.Gly92=
XM_006711529.2:c.274G=	XP_006711592.1:p.Gly92=
XM_005245483.3:c.274G=	XP_005245540.1:p.Gly92=
XM_017002298.1:c.274G=	XP_016857787.1:p.Gly92=
XM_017002299.1:c.274G=	XP_016857788.1:p.Gly92=
NM_001297575.2:c.274G=	NP_001284504.1:p.Gly92=
NM_014625.4:c.274G= MANE Select	NP_055440.1:p.Gly92=