Canonical Allele Identifier: CA2333851565
Gene: NPHS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35850882G= , CM000681.2:g.35850882G= GRCh38
NC_000019.9:g.36341784G= , CM000681.1:g.36341784G= GRCh37
NC_000019.8:g.41033624G= NCBI36
NG_013356.2:g.23406C= , LRG_693:g.23406C=
NG_051206.1:g.4248G=

Transcript Alleles

HGVS Amino-acid change
ENST00000378910.10:c.526+79C= MANE Select ENSP00000368190.4:n.526+79C=
ENST00000353632.6:c.526+79C= ENSP00000343634.5:n.526+79C=
ENST00000378910.9:c.526+79C= ENSP00000368190.4:n.526+79C=
NM_004646.3:c.526+79C= , LRG_693t1:c.526+79C= NP_004637.1:n.526+79C=
NM_004646.4:c.526+79C= MANE Select NP_004637.1:n.526+79C=
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