Canonical Allele Identifier: CA507314408
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1116390
ClinVar RCV Id: RCV001444731
dbSNP Id: rs2146826490
MyVariant Identifiers: chr19:g.36339177C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35848275C>T , CM000681.2:g.35848275C>T GRCh38
NC_000019.9:g.36339177C>T , CM000681.1:g.36339177C>T GRCh37
NC_000019.8:g.41031017C>T NCBI36
NG_013356.2:g.26013G>A , LRG_693:g.26013G>A
NG_051206.1:g.1641C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378910.10:c.1293G>A MANE Select ENSP00000368190.4:p.Lys431=
ENST00000353632.6:c.1293G>A ENSP00000343634.5:p.Lys431=
ENST00000378910.9:c.1293G>A ENSP00000368190.4:p.Lys431=
ENST00000592132.1:n.300G>A
NM_004646.3:c.1293G>A , LRG_693t1:c.1293G>A NP_004637.1:p.Lys431=
NM_004646.4:c.1293G>A MANE Select NP_004637.1:p.Lys431=
Search 100 bp 5'
Search 100 bp 3'