Canonical Allele Identifier: CA1210326815
Gene: NPHS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.179575962_179575963delinsCG , CM000663.2:g.179575962_179575963delinsCG GRCh38
NC_000001.10:g.179545097_179545098delinsCG , CM000663.1:g.179545097_179545098delinsCG GRCh37
NC_000001.9:g.177811720_177811721delinsCG NCBI36
NG_007535.1:g.4987_4988delinsCG , LRG_887:g.4987_4988delinsCG

Transcript Alleles

HGVS Amino-acid Change
XM_005245483.2:c.-99_-98delinsCG XP_005245540.1:n.-99_-98delinsCG
XM_006711529.2:c.-99_-98delinsCG XP_006711592.1:n.-99_-98delinsCG
XM_005245483.3:c.-99_-98delinsCG XP_005245540.1:n.-99_-98delinsCG
XM_017002298.1:c.-99_-98delinsCG XP_016857787.1:n.-99_-98delinsCG
XM_017002299.1:c.-99_-98delinsCG XP_016857788.1:n.-99_-98delinsCG