Canonical Allele Identifier: CA2333850830
Gene: NPHS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35849298T= , CM000681.2:g.35849298T= GRCh38
NC_000019.9:g.36340200T= , CM000681.1:g.36340200T= GRCh37
NC_000019.8:g.41032040T= NCBI36
NG_013356.2:g.24990A= , LRG_693:g.24990A=
NG_051206.1:g.2664T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378910.10:c.778A= MANE Select ENSP00000368190.4:p.Ser260=
ENST00000353632.6:c.778A= ENSP00000343634.5:p.Ser260=
ENST00000378910.9:c.778A= ENSP00000368190.4:p.Ser260=
NM_004646.3:c.778A= , LRG_693t1:c.778A= NP_004637.1:p.Ser260=
NM_004646.4:c.778A= MANE Select NP_004637.1:p.Ser260=