Canonical Allele Identifier: CA2333840011
Gene: NPHS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35826526T= , CM000681.2:g.35826526T= GRCh38
NC_000019.9:g.36317428T= , CM000681.1:g.36317428T= GRCh37
NC_000019.8:g.41009268T= NCBI36
NG_013356.2:g.47762A= , LRG_693:g.47762A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378910.10:c.3714A= MANE Select ENSP00000368190.4:p.Gly1238=
ENST00000353632.6:c.3594A= ENSP00000343634.5:p.Gly1198=
ENST00000378910.9:c.3714A= ENSP00000368190.4:p.Gly1238=
NM_004646.3:c.3714A= , LRG_693t1:c.3714A= NP_004637.1:p.Gly1238=
NM_004646.4:c.3714A= MANE Select NP_004637.1:p.Gly1238=