Canonical Allele Identifier: CA2333850691

Gene: NPHS1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35849015C= , CM000681.2:g.35849015C=	GRCh38
NC_000019.9:g.36339917C= , CM000681.1:g.36339917C=	GRCh37
NC_000019.8:g.41031757C=	NCBI36
NG_013356.2:g.25273G= , LRG_693:g.25273G=
NG_051206.1:g.2381C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378910.10:c.973G= MANE Select	ENSP00000368190.4:p.Ala325=
ENST00000353632.6:c.973G=	ENSP00000343634.5:p.Ala325=
ENST00000378910.9:c.973G=	ENSP00000368190.4:p.Ala325=
NM_004646.3:c.973G= , LRG_693t1:c.973G=	NP_004637.1:p.Ala325=
NM_004646.4:c.973G= MANE Select	NP_004637.1:p.Ala325=