Canonical Allele Identifier: CA2333839552
Gene: NPHS1 HGNC NCBI

Linked Data

dbSNP Id: rs1599833167

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35826705G>T , CM000681.2:g.35826705G>T GRCh38
NC_000019.9:g.36317607G>T , CM000681.1:g.36317607G>T GRCh37
NC_000019.8:g.41009447G>T NCBI36
NG_013356.2:g.47583C>A , LRG_693:g.47583C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378910.10:c.3595-60C>A MANE Select ENSP00000368190.4:n.3595-60C>A
ENST00000353632.6:c.3475-60C>A ENSP00000343634.5:n.3475-60C>A
ENST00000378910.9:c.3595-60C>A ENSP00000368190.4:n.3595-60C>A
NM_004646.3:c.3595-60C>A , LRG_693t1:c.3595-60C>A NP_004637.1:n.3595-60C>A
NM_004646.4:c.3595-60C>A MANE Select NP_004637.1:n.3595-60C>A