Canonical Allele Identifier: CA512663886
Gene: RIPK4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.43176811A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.41756651A>G , CM000683.2:g.41756651A>G GRCh38
NC_000021.8:g.43176811A>G , CM000683.1:g.43176811A>G GRCh37
NC_000021.7:g.42049880A>G NCBI36
NG_032113.1:g.15439T>C
NG_032113.2:g.15439T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000332512.8:c.348T>C MANE Select ENSP00000332454.3:p.Asp116=
ENST00000332512.7:c.348T>C ENSP00000332454.3:p.Asp116=
ENST00000352483.3:c.348T>C ENSP00000330161.2:p.Asp116=
NM_020639.2:c.348T>C NP_065690.2:p.Asp116=
NM_020639.3:c.348T>C MANE Select NP_065690.2:p.Asp116=
Search 100 bp 5'
Search 100 bp 3'