Canonical Allele Identifier: CA405385791
Gene: NPHS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.36330410C>G (hg19) chr19:g.35839508C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35839508C>G , CM000681.2:g.35839508C>G GRCh38
NC_000019.9:g.36330410C>G , CM000681.1:g.36330410C>G GRCh37
NC_000019.8:g.41022250C>G NCBI36
NG_013356.2:g.34780G>C , LRG_693:g.34780G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378910.10:c.2915G>C MANE Select ENSP00000368190.4:p.Arg972Thr
ENST00000353632.6:c.2915G>C ENSP00000343634.5:p.Arg972Thr
ENST00000378910.9:c.2915G>C ENSP00000368190.4:p.Arg972Thr
NM_004646.3:c.2915G>C , LRG_693t1:c.2915G>C NP_004637.1:p.Arg972Thr
NM_004646.4:c.2915G>C MANE Select NP_004637.1:p.Arg972Thr
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