Canonical Allele Identifier: CA507092674
Gene: NPHS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.36322031T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35831129T>C , CM000681.2:g.35831129T>C GRCh38
NC_000019.9:g.36322031T>C , CM000681.1:g.36322031T>C GRCh37
NC_000019.8:g.41013871T>C NCBI36
NG_013356.2:g.43159A>G , LRG_693:g.43159A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378910.10:c.3405A>G MANE Select ENSP00000368190.4:p.Ala1135=
ENST00000353632.6:c.3285A>G ENSP00000343634.5:p.Ala1095=
ENST00000378910.9:c.3405A>G ENSP00000368190.4:p.Ala1135=
NM_004646.3:c.3405A>G , LRG_693t1:c.3405A>G NP_004637.1:p.Ala1135=
NM_004646.4:c.3405A>G MANE Select NP_004637.1:p.Ala1135=