Canonical Allele Identifier: CA2649317192
Gene: NPHS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.179575954_179575955insACCCGCA , CM000663.2:g.179575954_179575955insACCCGCA GRCh38
NC_000001.10:g.179545089_179545090insACCCGCA , CM000663.1:g.179545089_179545090insACCCGCA GRCh37
NC_000001.9:g.177811712_177811713insACCCGCA NCBI36
NG_007535.1:g.4995_4996insTGCGGGT , LRG_887:g.4995_4996insTGCGGGT

Transcript Alleles

HGVS Amino-acid Change
XM_005245483.2:c.-91_-90insTGCGGGT XP_005245540.1:n.-91_-90insTGCGGGT
XM_006711529.2:c.-91_-90insTGCGGGT XP_006711592.1:n.-91_-90insTGCGGGT
XM_005245483.3:c.-91_-90insTGCGGGT XP_005245540.1:n.-91_-90insTGCGGGT
XM_017002298.1:c.-91_-90insTGCGGGT XP_016857787.1:n.-91_-90insTGCGGGT
XM_017002299.1:c.-91_-90insTGCGGGT XP_016857788.1:n.-91_-90insTGCGGGT