Canonical Allele Identifier: CA250240
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 56506
ClinVar RCV Id: RCV000049919
dbSNP Id: rs386833944
MyVariant Identifiers: chr19:g.36341910C>G (hg19) chr19:g.35851008C>G (hg38)
PubMed: PMID:19321760
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35851008C>G , CM000681.2:g.35851008C>G GRCh38
NC_000019.9:g.36341910C>G , CM000681.1:g.36341910C>G GRCh37
NC_000019.8:g.41033750C>G NCBI36
NG_013356.2:g.23280G>C , LRG_693:g.23280G>C
NG_051206.1:g.4374C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378910.10:c.479G>C MANE Select ENSP00000368190.4:p.Cys160Ser
ENST00000353632.6:c.479G>C ENSP00000343634.5:p.Cys160Ser
ENST00000378910.9:c.479G>C ENSP00000368190.4:p.Cys160Ser
NM_004646.3:c.479G>C , LRG_693t1:c.479G>C NP_004637.1:p.Cys160Ser
NM_004646.4:c.479G>C MANE Select NP_004637.1:p.Cys160Ser
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