Canonical Allele Identifier: CA1210319201

Gene: NPHS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179556929G= , CM000663.2:g.179556929G=	GRCh38
NC_000001.10:g.179526064G= , CM000663.1:g.179526064G=	GRCh37
NC_000001.9:g.177792687G=	NCBI36
NG_007535.1:g.24021C= , LRG_887:g.24021C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367615.9:c.738+98C= MANE Select	ENSP00000356587.4:n.738+98C=
ENST00000367615.8:c.738+98C=	ENSP00000356587.4:n.738+98C=
ENST00000367616.4:c.535-2398C=	ENSP00000356588.4:n.535-2398C=
NM_001297575.1:c.535-2398C=	NP_001284504.1:n.535-2398C=
NM_014625.3:c.738+98C= , LRG_887t1:c.738+98C=	NP_055440.1:n.738+98C=
XM_005245483.2:c.561+98C=	XP_005245540.1:n.561+98C=
XM_006711529.2:c.738+98C=	XP_006711592.1:n.738+98C=
XM_005245483.3:c.561+98C=	XP_005245540.1:n.561+98C=
XM_017002298.1:c.461+2750C=	XP_016857787.1:n.461+2750C=
XM_017002299.1:c.534+2750C=	XP_016857788.1:n.534+2750C=
NM_001297575.2:c.535-2398C=	NP_001284504.1:n.535-2398C=
NM_014625.4:c.738+98C= MANE Select	NP_055440.1:n.738+98C=