Canonical Allele Identifier: CA405407029
Gene: NPHS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35849255G>A , CM000681.2:g.35849255G>A GRCh38
NC_000019.9:g.36340157G>A , CM000681.1:g.36340157G>A GRCh37
NC_000019.8:g.41031997G>A NCBI36
NG_013356.2:g.25033C>T , LRG_693:g.25033C>T
NG_051206.1:g.2621G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378910.10:c.821C>T MANE Select ENSP00000368190.4:p.Ala274Val
ENST00000353632.6:c.821C>T ENSP00000343634.5:p.Ala274Val
ENST00000378910.9:c.821C>T ENSP00000368190.4:p.Ala274Val
NM_004646.3:c.821C>T , LRG_693t1:c.821C>T NP_004637.1:p.Ala274Val
NM_004646.4:c.821C>T MANE Select NP_004637.1:p.Ala274Val