Canonical Allele Identifier: CA2333850797

Gene: NPHS1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35849234A= , CM000681.2:g.35849234A=	GRCh38
NC_000019.9:g.36340136A= , CM000681.1:g.36340136A=	GRCh37
NC_000019.8:g.41031976A=	NCBI36
NG_013356.2:g.25054T= , LRG_693:g.25054T=
NG_051206.1:g.2600A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378910.10:c.840+2T= MANE Select	ENSP00000368190.4:n.840+2T=
ENST00000353632.6:c.840+2T=	ENSP00000343634.5:n.840+2T=
ENST00000378910.9:c.840+2T=	ENSP00000368190.4:n.840+2T=
NM_004646.3:c.840+2T= , LRG_693t1:c.840+2T=	NP_004637.1:n.840+2T=
NM_004646.4:c.840+2T= MANE Select	NP_004637.1:n.840+2T=