Canonical Allele Identifier: CA405407069
Gene: NPHS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.36340178G>C (hg19) chr19:g.35849276G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35849276G>C , CM000681.2:g.35849276G>C GRCh38
NC_000019.9:g.36340178G>C , CM000681.1:g.36340178G>C GRCh37
NC_000019.8:g.41032018G>C NCBI36
NG_013356.2:g.25012C>G , LRG_693:g.25012C>G
NG_051206.1:g.2642G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378910.10:c.800C>G MANE Select ENSP00000368190.4:p.Ala267Gly
ENST00000353632.6:c.800C>G ENSP00000343634.5:p.Ala267Gly
ENST00000378910.9:c.800C>G ENSP00000368190.4:p.Ala267Gly
NM_004646.3:c.800C>G , LRG_693t1:c.800C>G NP_004637.1:p.Ala267Gly
NM_004646.4:c.800C>G MANE Select NP_004637.1:p.Ala267Gly
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