Canonical Allele Identifier: CA2649317205
Gene: NPHS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.179575963_179575964insATGGTCTTTAGGGTCCCCC , CM000663.2:g.179575963_179575964insATGGTCTTTAGGGTCCCCC GRCh38
NC_000001.10:g.179545098_179545099insATGGTCTTTAGGGTCCCCC , CM000663.1:g.179545098_179545099insATGGTCTTTAGGGTCCCCC GRCh37
NC_000001.9:g.177811721_177811722insATGGTCTTTAGGGTCCCCC NCBI36
NG_007535.1:g.4986_4987insGGGGGACCCTAAAGACCAT , LRG_887:g.4986_4987insGGGGGACCCTAAAGACCAT

Transcript Alleles

HGVS Amino-acid Change
XM_005245483.2:c.-100_-99insGGGGGACCCTAAAGACCAT XP_005245540.1:n.-100_-99insGGGGGACCCTAAAGACCAT
XM_006711529.2:c.-100_-99insGGGGGACCCTAAAGACCAT XP_006711592.1:n.-100_-99insGGGGGACCCTAAAGACCAT
XM_005245483.3:c.-100_-99insGGGGGACCCTAAAGACCAT XP_005245540.1:n.-100_-99insGGGGGACCCTAAAGACCAT
XM_017002298.1:c.-100_-99insGGGGGACCCTAAAGACCAT XP_016857787.1:n.-100_-99insGGGGGACCCTAAAGACCAT
XM_017002299.1:c.-100_-99insGGGGGACCCTAAAGACCAT XP_016857788.1:n.-100_-99insGGGGGACCCTAAAGACCAT