Canonical Allele Identifier: CA405399775
Gene: NPHS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35845731C>A , CM000681.2:g.35845731C>A GRCh38
NC_000019.9:g.36336633C>A , CM000681.1:g.36336633C>A GRCh37
NC_000019.8:g.41028473C>A NCBI36
NG_013356.2:g.28557G>T , LRG_693:g.28557G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378910.10:c.1695G>T MANE Select ENSP00000368190.4:p.Leu565Phe
ENST00000353632.6:c.1695G>T ENSP00000343634.5:p.Leu565Phe
ENST00000378910.9:c.1695G>T ENSP00000368190.4:p.Leu565Phe
NM_004646.3:c.1695G>T , LRG_693t1:c.1695G>T NP_004637.1:p.Leu565Phe
NM_004646.4:c.1695G>T MANE Select NP_004637.1:p.Leu565Phe