Canonical Allele Identifier: CA405405889
Gene: NPHS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.36339287C>G (hg19) chr19:g.35848385C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35848385C>G , CM000681.2:g.35848385C>G GRCh38
NC_000019.9:g.36339287C>G , CM000681.1:g.36339287C>G GRCh37
NC_000019.8:g.41031127C>G NCBI36
NG_013356.2:g.25903G>C , LRG_693:g.25903G>C
NG_051206.1:g.1751C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378910.10:c.1183G>C MANE Select ENSP00000368190.4:p.Gly395Arg
ENST00000353632.6:c.1183G>C ENSP00000343634.5:p.Gly395Arg
ENST00000378910.9:c.1183G>C ENSP00000368190.4:p.Gly395Arg
ENST00000592132.1:n.190G>C
NM_004646.3:c.1183G>C , LRG_693t1:c.1183G>C NP_004637.1:p.Gly395Arg
NM_004646.4:c.1183G>C MANE Select NP_004637.1:p.Gly395Arg
Search 100 bp 5'
Search 100 bp 3'