Canonical Allele Identifier: CA1210319220
Gene: NPHS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.179557003T= , CM000663.2:g.179557003T= GRCh38
NC_000001.10:g.179526138T= , CM000663.1:g.179526138T= GRCh37
NC_000001.9:g.177792761T= NCBI36
NG_007535.1:g.23947A= , LRG_887:g.23947A=

Transcript Alleles

HGVS Amino-acid change
ENST00000367615.9:c.738+24A= MANE Select ENSP00000356587.4:n.738+24A=
ENST00000367615.8:c.738+24A= ENSP00000356587.4:n.738+24A=
ENST00000367616.4:c.535-2472A= ENSP00000356588.4:n.535-2472A=
NM_001297575.1:c.535-2472A= NP_001284504.1:n.535-2472A=
NM_014625.3:c.738+24A= , LRG_887t1:c.738+24A= NP_055440.1:n.738+24A=
XM_005245483.2:c.561+24A= XP_005245540.1:n.561+24A=
XM_006711529.2:c.738+24A= XP_006711592.1:n.738+24A=
XM_005245483.3:c.561+24A= XP_005245540.1:n.561+24A=
XM_017002298.1:c.461+2676A= XP_016857787.1:n.461+2676A=
XM_017002299.1:c.534+2676A= XP_016857788.1:n.534+2676A=
NM_001297575.2:c.535-2472A= NP_001284504.1:n.535-2472A=
NM_014625.4:c.738+24A= MANE Select NP_055440.1:n.738+24A=