Canonical Allele Identifier: CA916082456
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 836621
ClinVar RCV Id: RCV001037796
dbSNP Id: rs1973176439

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35848398del , CM000681.2:g.35848398del GRCh38
NC_000019.9:g.36339300del , CM000681.1:g.36339300del GRCh37
NC_000019.8:g.41031140del NCBI36
NG_013356.2:g.25892del , LRG_693:g.25892del
NG_051206.1:g.1764del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378910.10:c.1172del
ENST00000353632.6:c.1172del
ENST00000378910.9:c.1172del
ENST00000592132.1:n.179del
NM_004646.3:c.1172del , LRG_693t1:c.1172del
NM_004646.4:c.1172del