Canonical Allele Identifier: CA2333849213

Gene: NPHS1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35845972G= , CM000681.2:g.35845972G=	GRCh38
NC_000019.9:g.36336874G= , CM000681.1:g.36336874G=	GRCh37
NC_000019.8:g.41028714G=	NCBI36
NG_013356.2:g.28316C= , LRG_693:g.28316C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378910.10:c.1627+36C= MANE Select	ENSP00000368190.4:n.1627+36C=
ENST00000353632.6:c.1627+36C=	ENSP00000343634.5:n.1627+36C=
ENST00000378910.9:c.1627+36C=	ENSP00000368190.4:n.1627+36C=
NM_004646.3:c.1627+36C= , LRG_693t1:c.1627+36C=	NP_004637.1:n.1627+36C=
NM_004646.4:c.1627+36C= MANE Select	NP_004637.1:n.1627+36C=