Canonical Allele Identifier: CA2333849069

Gene: NPHS1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35845697T= , CM000681.2:g.35845697T=	GRCh38
NC_000019.9:g.36336599T= , CM000681.1:g.36336599T=	GRCh37
NC_000019.8:g.41028439T=	NCBI36
NG_013356.2:g.28591A= , LRG_693:g.28591A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000378910.10:c.1729A= MANE Select	ENSP00000368190.4:p.Asn577=
ENST00000353632.6:c.1729A=	ENSP00000343634.5:p.Asn577=
ENST00000378910.9:c.1729A=	ENSP00000368190.4:p.Asn577=
NM_004646.3:c.1729A= , LRG_693t1:c.1729A=	NP_004637.1:p.Asn577=
NM_004646.4:c.1729A= MANE Select	NP_004637.1:p.Asn577=