Canonical Allele Identifier: CA891821746

Gene: NPHS2

Linked Data

• dbSNP Id: rs1180435166
• MyVariant Identifiers: chr1:g.179534084_179534100del (hg19) ; chr1:g.179564949_179564965del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179564953_179564969del , CM000663.2:g.179564953_179564969del	GRCh38
NC_000001.10:g.179534088_179534104del , CM000663.1:g.179534088_179534104del	GRCh37
NC_000001.9:g.177800711_177800727del	NCBI36
NG_007535.1:g.15985_16001del , LRG_887:g.15985_16001del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367615.9:c.275-172_275-156del MANE Select	ENSP00000356587.4:n.275-172_275-156del
ENST00000367615.8:c.275-172_275-156del	ENSP00000356587.4:n.275-172_275-156del
ENST00000367616.4:c.275-172_275-156del	ENSP00000356588.4:n.275-172_275-156del
NM_001297575.1:c.275-172_275-156del	NP_001284504.1:n.275-172_275-156del
NM_014625.3:c.275-172_275-156del , LRG_887t1:c.275-172_275-156del	NP_055440.1:n.275-172_275-156del
XM_005245483.2:c.275-5204_275-5188del	XP_005245540.1:n.275-5204_275-5188del
XM_006711529.2:c.275-172_275-156del	XP_006711592.1:n.275-172_275-156del
XM_005245483.3:c.275-5204_275-5188del	XP_005245540.1:n.275-5204_275-5188del
XM_017002298.1:c.275-172_275-156del	XP_016857787.1:n.275-172_275-156del
XM_017002299.1:c.275-172_275-156del	XP_016857788.1:n.275-172_275-156del
NM_001297575.2:c.275-172_275-156del	NP_001284504.1:n.275-172_275-156del
NM_014625.4:c.275-172_275-156del MANE Select	NP_055440.1:n.275-172_275-156del