Canonical Allele Identifier: CA1147262198

Gene: NPHS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179556730G= , CM000663.2:g.179556730G=	GRCh38
NC_000001.10:g.179525865G= , CM000663.1:g.179525865G=	GRCh37
NC_000001.9:g.177792488G=	NCBI36
NG_007535.1:g.24220C= , LRG_887:g.24220C=
NG_033075.1:g.196011G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367615.9:c.738+297C= MANE Select	ENSP00000356587.4:n.738+297C=
ENST00000367615.8:c.738+297C=	ENSP00000356587.4:n.738+297C=
ENST00000367616.4:c.535-2199C=	ENSP00000356588.4:n.535-2199C=
NM_001297575.1:c.535-2199C=	NP_001284504.1:n.535-2199C=
NM_014625.3:c.738+297C= , LRG_887t1:c.738+297C=	NP_055440.1:n.738+297C=
XM_005245483.2:c.561+297C=	XP_005245540.1:n.561+297C=
XM_006711529.2:c.738+297C=	XP_006711592.1:n.738+297C=
XM_005245483.3:c.561+297C=	XP_005245540.1:n.561+297C=
XM_017002298.1:c.461+2949C=	XP_016857787.1:n.461+2949C=
XM_017002299.1:c.534+2949C=	XP_016857788.1:n.534+2949C=
NM_001297575.2:c.535-2199C=	NP_001284504.1:n.535-2199C=
NM_014625.4:c.738+297C= MANE Select	NP_055440.1:n.738+297C=