Canonical Allele Identifier: CA507314579
Gene: NPHS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.36340171C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35849269C>G , CM000681.2:g.35849269C>G GRCh38
NC_000019.9:g.36340171C>G , CM000681.1:g.36340171C>G GRCh37
NC_000019.8:g.41032011C>G NCBI36
NG_013356.2:g.25019G>C , LRG_693:g.25019G>C
NG_051206.1:g.2635C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378910.10:c.807G>C MANE Select ENSP00000368190.4:p.Gly269=
ENST00000353632.6:c.807G>C ENSP00000343634.5:p.Gly269=
ENST00000378910.9:c.807G>C ENSP00000368190.4:p.Gly269=
NM_004646.3:c.807G>C , LRG_693t1:c.807G>C NP_004637.1:p.Gly269=
NM_004646.4:c.807G>C MANE Select NP_004637.1:p.Gly269=