Canonical Allele Identifier: CA2584603979
Gene: NPHS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35849518C>T , CM000681.2:g.35849518C>T GRCh38
NC_000019.9:g.36340420C>T , CM000681.1:g.36340420C>T GRCh37
NC_000019.8:g.41032260C>T NCBI36
NG_013356.2:g.24770G>A , LRG_693:g.24770G>A
NG_051206.1:g.2884C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378910.10:c.712+32G>A MANE Select ENSP00000368190.4:n.712+32G>A
ENST00000353632.6:c.712+32G>A ENSP00000343634.5:n.712+32G>A
ENST00000378910.9:c.712+32G>A ENSP00000368190.4:n.712+32G>A
NM_004646.3:c.712+32G>A , LRG_693t1:c.712+32G>A NP_004637.1:n.712+32G>A
NM_004646.4:c.712+32G>A MANE Select NP_004637.1:n.712+32G>A