Canonical Allele Identifier: CA2333849906
Gene: NPHS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35848116G= , CM000681.2:g.35848116G= GRCh38
NC_000019.9:g.36339018G= , CM000681.1:g.36339018G= GRCh37
NC_000019.8:g.41030858G= NCBI36
NG_013356.2:g.26172C= , LRG_693:g.26172C=
NG_051206.1:g.1482G=

Transcript Alleles

HGVS Amino-acid change
ENST00000378910.10:c.1365C= MANE Select ENSP00000368190.4:p.Leu455=
ENST00000353632.6:c.1365C= ENSP00000343634.5:p.Leu455=
ENST00000378910.9:c.1365C= ENSP00000368190.4:p.Leu455=
ENST00000592132.1:n.372C=
NM_004646.3:c.1365C= , LRG_693t1:c.1365C= NP_004637.1:p.Leu455=
NM_004646.4:c.1365C= MANE Select NP_004637.1:p.Leu455=