Canonical Allele Identifier: CA343569657

Gene: NPHS2

Linked Data

• MyVariant Identifiers: chr1:g.179530454G>C (hg19) ; chr1:g.179561319G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179561319G>C , CM000663.2:g.179561319G>C	GRCh38
NC_000001.10:g.179530454G>C , CM000663.1:g.179530454G>C	GRCh37
NC_000001.9:g.177797077G>C	NCBI36
NG_007535.1:g.19631C>G , LRG_887:g.19631C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367615.9:c.421C>G MANE Select	ENSP00000356587.4:p.His141Asp
ENST00000367615.8:c.421C>G	ENSP00000356587.4:p.His141Asp
ENST00000367616.4:c.421C>G	ENSP00000356588.4:p.His141Asp
NM_001297575.1:c.421C>G	NP_001284504.1:p.His141Asp
NM_014625.3:c.421C>G , LRG_887t1:c.421C>G	NP_055440.1:p.His141Asp
XM_005245483.2:c.275-1558C>G	XP_005245540.1:n.275-1558C>G
XM_006711529.2:c.421C>G	XP_006711592.1:p.His141Asp
XM_005245483.3:c.275-1558C>G	XP_005245540.1:n.275-1558C>G
XM_017002298.1:c.379-1558C>G	XP_016857787.1:n.379-1558C>G
XM_017002299.1:c.421C>G	XP_016857788.1:p.His141Asp
NM_001297575.2:c.421C>G	NP_001284504.1:p.His141Asp
NM_014625.4:c.421C>G MANE Select	NP_055440.1:p.His141Asp