Canonical Allele Identifier: CA2333850587
Gene: NPHS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35848828G= , CM000681.2:g.35848828G= GRCh38
NC_000019.9:g.36339730G= , CM000681.1:g.36339730G= GRCh37
NC_000019.8:g.41031570G= NCBI36
NG_013356.2:g.25460C= , LRG_693:g.25460C=
NG_051206.1:g.2194G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378910.10:c.1013-34C= MANE Select ENSP00000368190.4:n.1013-34C=
ENST00000353632.6:c.1013-34C= ENSP00000343634.5:n.1013-34C=
ENST00000378910.9:c.1013-34C= ENSP00000368190.4:n.1013-34C=
ENST00000592132.1:n.20-34C=
NM_004646.3:c.1013-34C= , LRG_693t1:c.1013-34C= NP_004637.1:n.1013-34C=
NM_004646.4:c.1013-34C= MANE Select NP_004637.1:n.1013-34C=
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