Canonical Allele Identifier: CA2584603202
Gene: NPHS1 HGNC NCBI

Linked Data

gnomAD v4: 19-35845598-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35845598A>G , CM000681.2:g.35845598A>G GRCh38
NC_000019.9:g.36336500A>G , CM000681.1:g.36336500A>G GRCh37
NC_000019.8:g.41028340A>G NCBI36
NG_013356.2:g.28690T>C , LRG_693:g.28690T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378910.10:c.1758-58T>C MANE Select ENSP00000368190.4:n.1758-58T>C
ENST00000353632.6:c.1758-58T>C ENSP00000343634.5:n.1758-58T>C
ENST00000378910.9:c.1758-58T>C ENSP00000368190.4:n.1758-58T>C
NM_004646.3:c.1758-58T>C , LRG_693t1:c.1758-58T>C NP_004637.1:n.1758-58T>C
NM_004646.4:c.1758-58T>C MANE Select NP_004637.1:n.1758-58T>C
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