Canonical Allele Identifier: CA405415053
Gene: NPHS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.36317453T>A (hg19) chr19:g.35826551T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35826551T>A , CM000681.2:g.35826551T>A GRCh38
NC_000019.9:g.36317453T>A , CM000681.1:g.36317453T>A GRCh37
NC_000019.8:g.41009293T>A NCBI36
NG_013356.2:g.47737A>T , LRG_693:g.47737A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378910.10:c.3689A>T MANE Select ENSP00000368190.4:p.Asp1230Val
ENST00000353632.6:c.3569A>T ENSP00000343634.5:p.Asp1190Val
ENST00000378910.9:c.3689A>T ENSP00000368190.4:p.Asp1230Val
NM_004646.3:c.3689A>T , LRG_693t1:c.3689A>T NP_004637.1:p.Asp1230Val
NM_004646.4:c.3689A>T MANE Select NP_004637.1:p.Asp1230Val
Search 100 bp 5'
Search 100 bp 3'