Canonical Allele Identifier: CA1210319038

Gene: NPHS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179556555A= , CM000663.2:g.179556555A=	GRCh38
NC_000001.10:g.179525690A= , CM000663.1:g.179525690A=	GRCh37
NC_000001.9:g.177792313A=	NCBI36
NG_007535.1:g.24395T= , LRG_887:g.24395T=
NG_033075.1:g.195836A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367615.9:c.738+472T= MANE Select	ENSP00000356587.4:n.738+472T=
ENST00000367615.8:c.738+472T=	ENSP00000356587.4:n.738+472T=
ENST00000367616.4:c.535-2024T=	ENSP00000356588.4:n.535-2024T=
NM_001297575.1:c.535-2024T=	NP_001284504.1:n.535-2024T=
NM_014625.3:c.738+472T= , LRG_887t1:c.738+472T=	NP_055440.1:n.738+472T=
XM_005245483.2:c.561+472T=	XP_005245540.1:n.561+472T=
XM_006711529.2:c.738+472T=	XP_006711592.1:n.738+472T=
XM_005245483.3:c.561+472T=	XP_005245540.1:n.561+472T=
XM_017002298.1:c.461+3124T=	XP_016857787.1:n.461+3124T=
XM_017002299.1:c.534+3124T=	XP_016857788.1:n.534+3124T=
NM_001297575.2:c.535-2024T=	NP_001284504.1:n.535-2024T=
NM_014625.4:c.738+472T= MANE Select	NP_055440.1:n.738+472T=