Canonical Allele Identifier: CA507314348
Gene: NPHS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.36339021C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35848119C>T , CM000681.2:g.35848119C>T GRCh38
NC_000019.9:g.36339021C>T , CM000681.1:g.36339021C>T GRCh37
NC_000019.8:g.41030861C>T NCBI36
NG_013356.2:g.26169G>A , LRG_693:g.26169G>A
NG_051206.1:g.1485C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378910.10:c.1362G>A MANE Select ENSP00000368190.4:p.Lys454=
ENST00000353632.6:c.1362G>A ENSP00000343634.5:p.Lys454=
ENST00000378910.9:c.1362G>A ENSP00000368190.4:p.Lys454=
ENST00000592132.1:n.369G>A
NM_004646.3:c.1362G>A , LRG_693t1:c.1362G>A NP_004637.1:p.Lys454=
NM_004646.4:c.1362G>A MANE Select NP_004637.1:p.Lys454=