Canonical Allele Identifier: CA507092676
Gene: NPHS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.36322031T>G (hg19)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000378910.10:c.3405A>C MANE Select ENSP00000368190.4:p.Ala1135=
ENST00000353632.6:c.3285A>C ENSP00000343634.5:p.Ala1095=
ENST00000378910.9:c.3405A>C ENSP00000368190.4:p.Ala1135=
NM_004646.3:c.3405A>C , LRG_693t1:c.3405A>C NP_004637.1:p.Ala1135=
NM_004646.4:c.3405A>C MANE Select NP_004637.1:p.Ala1135=
Search 100 bp 5'
Search 100 bp 3'