Canonical Allele Identifier: CA2499225442
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1079137
ClinVar RCV Id: RCV001394290
dbSNP Id: rs2146807165

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35831046A>C , CM000681.2:g.35831046A>C GRCh38
NC_000019.9:g.36321948A>C , CM000681.1:g.36321948A>C GRCh37
NC_000019.8:g.41013788A>C NCBI36
NG_013356.2:g.43242T>G , LRG_693:g.43242T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378910.10:c.3481+7T>G MANE Select ENSP00000368190.4:n.3481+7T>G
ENST00000353632.6:c.3361+7T>G ENSP00000343634.5:n.3361+7T>G
ENST00000378910.9:c.3481+7T>G ENSP00000368190.4:n.3481+7T>G
NM_004646.3:c.3481+7T>G , LRG_693t1:c.3481+7T>G NP_004637.1:n.3481+7T>G
NM_004646.4:c.3481+7T>G MANE Select NP_004637.1:n.3481+7T>G