Canonical Allele Identifier: CA343568150

Gene: NPHS2

Linked Data

• MyVariant Identifiers: chr1:g.179526323A>G (hg19) ; chr1:g.179557188A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179557188A>G , CM000663.2:g.179557188A>G	GRCh38
NC_000001.10:g.179526323A>G , CM000663.1:g.179526323A>G	GRCh37
NC_000001.9:g.177792946A>G	NCBI36
NG_007535.1:g.23762T>C , LRG_887:g.23762T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367615.9:c.577T>C MANE Select	ENSP00000356587.4:p.Cys193Arg
ENST00000367615.8:c.577T>C	ENSP00000356587.4:p.Cys193Arg
ENST00000367616.4:c.534+2491T>C	ENSP00000356588.4:n.534+2491T>C
NM_001297575.1:c.534+2491T>C	NP_001284504.1:n.534+2491T>C
NM_014625.3:c.577T>C , LRG_887t1:c.577T>C	NP_055440.1:p.Cys193Arg
XM_005245483.2:c.400T>C	XP_005245540.1:p.Cys134Arg
XM_006711529.2:c.577T>C	XP_006711592.1:p.Cys193Arg
XM_005245483.3:c.400T>C	XP_005245540.1:p.Cys134Arg
XM_017002298.1:c.461+2491T>C	XP_016857787.1:n.461+2491T>C
XM_017002299.1:c.534+2491T>C	XP_016857788.1:n.534+2491T>C
NM_001297575.2:c.534+2491T>C	NP_001284504.1:n.534+2491T>C
NM_014625.4:c.577T>C MANE Select	NP_055440.1:p.Cys193Arg