Canonical Allele Identifier: CA2649316342

Gene: NPHS2

Linked Data

• gnomAD v4: 1-179561253-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179561253A>G , CM000663.2:g.179561253A>G	GRCh38
NC_000001.10:g.179530388A>G , CM000663.1:g.179530388A>G	GRCh37
NC_000001.9:g.177797011A>G	NCBI36
NG_007535.1:g.19697T>C , LRG_887:g.19697T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367615.9:c.451+36T>C MANE Select	ENSP00000356587.4:n.451+36T>C
ENST00000367615.8:c.451+36T>C	ENSP00000356587.4:n.451+36T>C
ENST00000367616.4:c.451+36T>C	ENSP00000356588.4:n.451+36T>C
NM_001297575.1:c.451+36T>C	NP_001284504.1:n.451+36T>C
NM_014625.3:c.451+36T>C , LRG_887t1:c.451+36T>C	NP_055440.1:n.451+36T>C
XM_005245483.2:c.275-1492T>C	XP_005245540.1:n.275-1492T>C
XM_006711529.2:c.451+36T>C	XP_006711592.1:n.451+36T>C
XM_005245483.3:c.275-1492T>C	XP_005245540.1:n.275-1492T>C
XM_017002298.1:c.379-1492T>C	XP_016857787.1:n.379-1492T>C
XM_017002299.1:c.451+36T>C	XP_016857788.1:n.451+36T>C
NM_001297575.2:c.451+36T>C	NP_001284504.1:n.451+36T>C
NM_014625.4:c.451+36T>C MANE Select	NP_055440.1:n.451+36T>C