Canonical Allele Identifier: CA405400131
Gene: NPHS1 HGNC NCBI

Linked Data

dbSNP Id: rs1392331476

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35846021C>G , CM000681.2:g.35846021C>G GRCh38
NC_000019.9:g.36336923C>G , CM000681.1:g.36336923C>G GRCh37
NC_000019.8:g.41028763C>G NCBI36
NG_013356.2:g.28267G>C , LRG_693:g.28267G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378910.10:c.1614G>C MANE Select ENSP00000368190.4:p.Gln538His
ENST00000353632.6:c.1614G>C ENSP00000343634.5:p.Gln538His
ENST00000378910.9:c.1614G>C ENSP00000368190.4:p.Gln538His
NM_004646.3:c.1614G>C , LRG_693t1:c.1614G>C NP_004637.1:p.Gln538His
NM_004646.4:c.1614G>C MANE Select NP_004637.1:p.Gln538His