Canonical Allele Identifier: CA2584603704
Gene: NPHS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35848503dup , CM000681.2:g.35848503dup GRCh38
NC_000019.9:g.36339405dup , CM000681.1:g.36339405dup GRCh37
NC_000019.8:g.41031245dup NCBI36
NG_013356.2:g.25785dup , LRG_693:g.25785dup
NG_051206.1:g.1869dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000378910.10:c.1171-106dup MANE Select ENSP00000368190.4:n.1171-106dup
ENST00000353632.6:c.1171-106dup ENSP00000343634.5:n.1171-106dup
ENST00000378910.9:c.1171-106dup ENSP00000368190.4:n.1171-106dup
ENST00000592132.1:n.178-106dup
NM_004646.3:c.1171-106dup , LRG_693t1:c.1171-106dup NP_004637.1:n.1171-106dup
NM_004646.4:c.1171-106dup MANE Select NP_004637.1:n.1171-106dup