Canonical Allele Identifier: CA405385774
Gene: NPHS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35839506A>T , CM000681.2:g.35839506A>T GRCh38
NC_000019.9:g.36330408A>T , CM000681.1:g.36330408A>T GRCh37
NC_000019.8:g.41022248A>T NCBI36
NG_013356.2:g.34782T>A , LRG_693:g.34782T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378910.10:c.2917T>A MANE Select ENSP00000368190.4:p.Phe973Ile
ENST00000353632.6:c.2917T>A ENSP00000343634.5:p.Phe973Ile
ENST00000378910.9:c.2917T>A ENSP00000368190.4:p.Phe973Ile
NM_004646.3:c.2917T>A , LRG_693t1:c.2917T>A NP_004637.1:p.Phe973Ile
NM_004646.4:c.2917T>A MANE Select NP_004637.1:p.Phe973Ile