Canonical Allele Identifier: CA2333849260
Gene: NPHS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35846042T= , CM000681.2:g.35846042T= GRCh38
NC_000019.9:g.36336944T= , CM000681.1:g.36336944T= GRCh37
NC_000019.8:g.41028784T= NCBI36
NG_013356.2:g.28246A= , LRG_693:g.28246A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378910.10:c.1593A= MANE Select ENSP00000368190.4:p.Gly531=
ENST00000353632.6:c.1593A= ENSP00000343634.5:p.Gly531=
ENST00000378910.9:c.1593A= ENSP00000368190.4:p.Gly531=
NM_004646.3:c.1593A= , LRG_693t1:c.1593A= NP_004637.1:p.Gly531=
NM_004646.4:c.1593A= MANE Select NP_004637.1:p.Gly531=
Search 100 bp 5'
Search 100 bp 3'