Canonical Allele Identifier: CA2838873360
Gene: NPHS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35849435del , CM000681.2:g.35849435del GRCh38
NC_000019.9:g.36340337del , CM000681.1:g.36340337del GRCh37
NC_000019.8:g.41032177del NCBI36
NG_013356.2:g.24855del , LRG_693:g.24855del
NG_051206.1:g.2801del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378910.10:c.713-70del MANE Select ENSP00000368190.4:n.713-70del
ENST00000353632.6:c.713-70del ENSP00000343634.5:n.713-70del
ENST00000378910.9:c.713-70del ENSP00000368190.4:n.713-70del
NM_004646.3:c.713-70del , LRG_693t1:c.713-70del NP_004637.1:n.713-70del
NM_004646.4:c.713-70del MANE Select NP_004637.1:n.713-70del