Canonical Allele Identifier: CA2649317135

Gene: NPHS2

Linked Data

• gnomAD v4: 1-179575920-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179575920G>C , CM000663.2:g.179575920G>C	GRCh38
NC_000001.10:g.179545055G>C , CM000663.1:g.179545055G>C	GRCh37
NC_000001.9:g.177811678G>C	NCBI36
NG_007535.1:g.5030C>G , LRG_887:g.5030C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367615.9:c.-56C>G MANE Select	ENSP00000356587.4:n.-56C>G
ENST00000367615.8:c.-56C>G	ENSP00000356587.4:n.-56C>G
ENST00000367616.4:c.-56C>G	ENSP00000356588.4:n.-56C>G
NM_001297575.1:c.-56C>G	NP_001284504.1:n.-56C>G
NM_014625.3:c.-56C>G , LRG_887t1:c.-56C>G	NP_055440.1:n.-56C>G
XM_005245483.2:c.-56C>G	XP_005245540.1:n.-56C>G
XM_006711529.2:c.-56C>G	XP_006711592.1:n.-56C>G
XM_005245483.3:c.-56C>G	XP_005245540.1:n.-56C>G
XM_017002298.1:c.-56C>G	XP_016857787.1:n.-56C>G
XM_017002299.1:c.-56C>G	XP_016857788.1:n.-56C>G
NM_001297575.2:c.-56C>G	NP_001284504.1:n.-56C>G
NM_014625.4:c.-56C>G MANE Select	NP_055440.1:n.-56C>G