Canonical Allele Identifier: CA2584603361

Gene: NPHS1

Linked Data

• gnomAD v4: 19-35845982-CGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35845984_35845985del , CM000681.2:g.35845984_35845985del	GRCh38
NC_000019.9:g.36336886_36336887del , CM000681.1:g.36336886_36336887del	GRCh37
NC_000019.8:g.41028726_41028727del	NCBI36
NG_013356.2:g.28304_28305del , LRG_693:g.28304_28305del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378910.10:c.1627+24_1627+25del MANE Select	ENSP00000368190.4:n.1627+24_1627+25del
ENST00000353632.6:c.1627+24_1627+25del	ENSP00000343634.5:n.1627+24_1627+25del
ENST00000378910.9:c.1627+24_1627+25del	ENSP00000368190.4:n.1627+24_1627+25del
NM_004646.3:c.1627+24_1627+25del , LRG_693t1:c.1627+24_1627+25del	NP_004637.1:n.1627+24_1627+25del
NM_004646.4:c.1627+24_1627+25del MANE Select	NP_004637.1:n.1627+24_1627+25del