Canonical Allele Identifier: CA405403729
Gene: NPHS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35848069T>G , CM000681.2:g.35848069T>G GRCh38
NC_000019.9:g.36338971T>G , CM000681.1:g.36338971T>G GRCh37
NC_000019.8:g.41030811T>G NCBI36
NG_013356.2:g.26219A>C , LRG_693:g.26219A>C
NG_051206.1:g.1435T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378910.10:c.1412A>C MANE Select ENSP00000368190.4:p.Asn471Thr
ENST00000353632.6:c.1412A>C ENSP00000343634.5:p.Asn471Thr
ENST00000378910.9:c.1412A>C ENSP00000368190.4:p.Asn471Thr
ENST00000592132.1:n.419A>C
NM_004646.3:c.1412A>C , LRG_693t1:c.1412A>C NP_004637.1:p.Asn471Thr
NM_004646.4:c.1412A>C MANE Select NP_004637.1:p.Asn471Thr