Canonical Allele Identifier: CA405400149
Gene: NPHS1 HGNC NCBI

Linked Data

dbSNP Id: rs1388452914

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35846031G>A , CM000681.2:g.35846031G>A GRCh38
NC_000019.9:g.36336933G>A , CM000681.1:g.36336933G>A GRCh37
NC_000019.8:g.41028773G>A NCBI36
NG_013356.2:g.28257C>T , LRG_693:g.28257C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378910.10:c.1604C>T MANE Select ENSP00000368190.4:p.Ala535Val
ENST00000353632.6:c.1604C>T ENSP00000343634.5:p.Ala535Val
ENST00000378910.9:c.1604C>T ENSP00000368190.4:p.Ala535Val
NM_004646.3:c.1604C>T , LRG_693t1:c.1604C>T NP_004637.1:p.Ala535Val
NM_004646.4:c.1604C>T MANE Select NP_004637.1:p.Ala535Val