Canonical Allele Identifier: CA2649316210

Gene: NPHS2

Linked Data

• gnomAD v4: 1-179559880-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179559880A>T , CM000663.2:g.179559880A>T	GRCh38
NC_000001.10:g.179529015A>T , CM000663.1:g.179529015A>T	GRCh37
NC_000001.9:g.177795638A>T	NCBI36
NG_007535.1:g.21070T>A , LRG_887:g.21070T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367615.9:c.452-119T>A MANE Select	ENSP00000356587.4:n.452-119T>A
ENST00000367615.8:c.452-119T>A	ENSP00000356587.4:n.452-119T>A
ENST00000367616.4:c.452-119T>A	ENSP00000356588.4:n.452-119T>A
NM_001297575.1:c.452-119T>A	NP_001284504.1:n.452-119T>A
NM_014625.3:c.452-119T>A , LRG_887t1:c.452-119T>A	NP_055440.1:n.452-119T>A
XM_005245483.2:c.275-119T>A	XP_005245540.1:n.275-119T>A
XM_006711529.2:c.452-119T>A	XP_006711592.1:n.452-119T>A
XM_005245483.3:c.275-119T>A	XP_005245540.1:n.275-119T>A
XM_017002298.1:c.379-119T>A	XP_016857787.1:n.379-119T>A
XM_017002299.1:c.452-119T>A	XP_016857788.1:n.452-119T>A
NM_001297575.2:c.452-119T>A	NP_001284504.1:n.452-119T>A
NM_014625.4:c.452-119T>A MANE Select	NP_055440.1:n.452-119T>A