Canonical Allele Identifier: CA10035798
Gene: RIPK4 HGNC NCBI

Linked Data

dbSNP Id: rs749072810

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.41756673G>A , CM000683.2:g.41756673G>A GRCh38
NC_000021.8:g.43176833G>A , CM000683.1:g.43176833G>A GRCh37
NC_000021.7:g.42049902G>A NCBI36
NG_032113.1:g.15417C>T
NG_032113.2:g.15417C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000332512.8:c.326C>T MANE Select ENSP00000332454.3:p.Ala109Val
ENST00000332512.7:c.326C>T ENSP00000332454.3:p.Ala109Val
ENST00000352483.3:c.326C>T ENSP00000330161.2:p.Ala109Val
NM_020639.2:c.326C>T NP_065690.2:p.Ala109Val
NM_020639.3:c.326C>T MANE Select NP_065690.2:p.Ala109Val