Canonical Allele Identifier: CA2333851590

Gene: NPHS1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35850952C= , CM000681.2:g.35850952C=	GRCh38
NC_000019.9:g.36341854C= , CM000681.1:g.36341854C=	GRCh37
NC_000019.8:g.41033694C=	NCBI36
NG_013356.2:g.23336G= , LRG_693:g.23336G=
NG_051206.1:g.4318C=

Transcript Alleles

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