Canonical Allele Identifier: CA2333849907
Gene: NPHS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35848118G= , CM000681.2:g.35848118G= GRCh38
NC_000019.9:g.36339020G= , CM000681.1:g.36339020G= GRCh37
NC_000019.8:g.41030860G= NCBI36
NG_013356.2:g.26170C= , LRG_693:g.26170C=
NG_051206.1:g.1484G=

Transcript Alleles

HGVS Amino-acid change
ENST00000378910.10:c.1363C= MANE Select ENSP00000368190.4:p.Leu455=
ENST00000353632.6:c.1363C= ENSP00000343634.5:p.Leu455=
ENST00000378910.9:c.1363C= ENSP00000368190.4:p.Leu455=
ENST00000592132.1:n.370C=
NM_004646.3:c.1363C= , LRG_693t1:c.1363C= NP_004637.1:p.Leu455=
NM_004646.4:c.1363C= MANE Select NP_004637.1:p.Leu455=