Canonical Allele Identifier: CA2333841978

Gene: NPHS1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35831035G= , CM000681.2:g.35831035G=	GRCh38
NC_000019.9:g.36321937G= , CM000681.1:g.36321937G=	GRCh37
NC_000019.8:g.41013777G=	NCBI36
NG_013356.2:g.43253C= , LRG_693:g.43253C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378910.10:c.3481+18C= MANE Select	ENSP00000368190.4:n.3481+18C=
ENST00000353632.6:c.3361+18C=	ENSP00000343634.5:n.3361+18C=
ENST00000378910.9:c.3481+18C=	ENSP00000368190.4:n.3481+18C=
NM_004646.3:c.3481+18C= , LRG_693t1:c.3481+18C=	NP_004637.1:n.3481+18C=
NM_004646.4:c.3481+18C= MANE Select	NP_004637.1:n.3481+18C=