Canonical Allele Identifier: CA2649317134

Gene: NPHS2

Linked Data

• gnomAD v4: 1-179575919-AGC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179575922_179575923del , CM000663.2:g.179575922_179575923del	GRCh38
NC_000001.10:g.179545057_179545058del , CM000663.1:g.179545057_179545058del	GRCh37
NC_000001.9:g.177811680_177811681del	NCBI36
NG_007535.1:g.5029_5030del , LRG_887:g.5029_5030del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367615.9:c.-57_-56del MANE Select	ENSP00000356587.4:n.-57_-56del
ENST00000367615.8:c.-57_-56del	ENSP00000356587.4:n.-57_-56del
ENST00000367616.4:c.-57_-56del	ENSP00000356588.4:n.-57_-56del
NM_001297575.1:c.-57_-56del	NP_001284504.1:n.-57_-56del
NM_014625.3:c.-57_-56del , LRG_887t1:c.-57_-56del	NP_055440.1:n.-57_-56del
XM_005245483.2:c.-57_-56del	XP_005245540.1:n.-57_-56del
XM_006711529.2:c.-57_-56del	XP_006711592.1:n.-57_-56del
XM_005245483.3:c.-57_-56del	XP_005245540.1:n.-57_-56del
XM_017002298.1:c.-57_-56del	XP_016857787.1:n.-57_-56del
XM_017002299.1:c.-57_-56del	XP_016857788.1:n.-57_-56del
NM_001297575.2:c.-57_-56del	NP_001284504.1:n.-57_-56del
NM_014625.4:c.-57_-56del MANE Select	NP_055440.1:n.-57_-56del