Canonical Allele Identifier: CA2333851555

Gene: NPHS1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35850844C= , CM000681.2:g.35850844C=	GRCh38
NC_000019.9:g.36341746C= , CM000681.1:g.36341746C=	GRCh37
NC_000019.8:g.41033586C=	NCBI36
NG_013356.2:g.23444G= , LRG_693:g.23444G=
NG_051206.1:g.4210C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378910.10:c.526+117G= MANE Select	ENSP00000368190.4:n.526+117G=
ENST00000353632.6:c.526+117G=	ENSP00000343634.5:n.526+117G=
ENST00000378910.9:c.526+117G=	ENSP00000368190.4:n.526+117G=
NM_004646.3:c.526+117G= , LRG_693t1:c.526+117G=	NP_004637.1:n.526+117G=
NM_004646.4:c.526+117G= MANE Select	NP_004637.1:n.526+117G=