Canonical Allele Identifier: CA2333850688

Gene: NPHS1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35849007G= , CM000681.2:g.35849007G=	GRCh38
NC_000019.9:g.36339909G= , CM000681.1:g.36339909G=	GRCh37
NC_000019.8:g.41031749G=	NCBI36
NG_013356.2:g.25281C= , LRG_693:g.25281C=
NG_051206.1:g.2373G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378910.10:c.981C= MANE Select	ENSP00000368190.4:p.Thr327=
ENST00000353632.6:c.981C=	ENSP00000343634.5:p.Thr327=
ENST00000378910.9:c.981C=	ENSP00000368190.4:p.Thr327=
NM_004646.3:c.981C= , LRG_693t1:c.981C=	NP_004637.1:p.Thr327=
NM_004646.4:c.981C= MANE Select	NP_004637.1:p.Thr327=