Canonical Allele Identifier: CA343571176
Gene: NPHS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.179564791T>C , CM000663.2:g.179564791T>C GRCh38
NC_000001.10:g.179533926T>C , CM000663.1:g.179533926T>C GRCh37
NC_000001.9:g.177800549T>C NCBI36
NG_007535.1:g.16159A>G , LRG_887:g.16159A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367615.9:c.277A>G MANE Select ENSP00000356587.4:p.Thr93Ala
ENST00000367615.8:c.277A>G ENSP00000356587.4:p.Thr93Ala
ENST00000367616.4:c.277A>G ENSP00000356588.4:p.Thr93Ala
NM_001297575.1:c.277A>G NP_001284504.1:p.Thr93Ala
NM_014625.3:c.277A>G , LRG_887t1:c.277A>G NP_055440.1:p.Thr93Ala
XM_005245483.2:c.275-5030A>G XP_005245540.1:n.275-5030A>G
XM_006711529.2:c.277A>G XP_006711592.1:p.Thr93Ala
XM_005245483.3:c.275-5030A>G XP_005245540.1:n.275-5030A>G
XM_017002298.1:c.277A>G XP_016857787.1:p.Thr93Ala
XM_017002299.1:c.277A>G XP_016857788.1:p.Thr93Ala
NM_001297575.2:c.277A>G NP_001284504.1:p.Thr93Ala
NM_014625.4:c.277A>G MANE Select NP_055440.1:p.Thr93Ala