Canonical Allele Identifier: CA421997375

Gene: NPHS2

Linked Data

• gnomAD v4: 1-179575766-G-C
• MyVariant Identifiers: chr1:g.179544901G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179575766G>C , CM000663.2:g.179575766G>C	GRCh38
NC_000001.10:g.179544901G>C , CM000663.1:g.179544901G>C	GRCh37
NC_000001.9:g.177811524G>C	NCBI36
NG_007535.1:g.5184C>G , LRG_887:g.5184C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367615.9:c.99C>G MANE Select	ENSP00000356587.4:p.Gly33=
ENST00000367615.8:c.99C>G	ENSP00000356587.4:p.Gly33=
ENST00000367616.4:c.99C>G	ENSP00000356588.4:p.Gly33=
NM_001297575.1:c.99C>G	NP_001284504.1:p.Gly33=
NM_014625.3:c.99C>G , LRG_887t1:c.99C>G	NP_055440.1:p.Gly33=
XM_005245483.2:c.99C>G	XP_005245540.1:p.Gly33=
XM_006711529.2:c.99C>G	XP_006711592.1:p.Gly33=
XM_005245483.3:c.99C>G	XP_005245540.1:p.Gly33=
XM_017002298.1:c.99C>G	XP_016857787.1:p.Gly33=
XM_017002299.1:c.99C>G	XP_016857788.1:p.Gly33=
NM_001297575.2:c.99C>G	NP_001284504.1:p.Gly33=
NM_014625.4:c.99C>G MANE Select	NP_055440.1:p.Gly33=