Canonical Allele Identifier: CA512662898
Gene: RIPK4 HGNC NCBI

Linked Data

gnomAD v4: 21-41741159-G-T
MyVariant Identifiers: chr21:g.43161319G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.41741159G>T , CM000683.2:g.41741159G>T GRCh38
NC_000021.8:g.43161319G>T , CM000683.1:g.43161319G>T GRCh37
NC_000021.7:g.42034388G>T NCBI36
NG_032113.1:g.30931C>A
NG_032113.2:g.30931C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000332512.8:c.2034C>A MANE Select ENSP00000332454.3:p.Ala678=
ENST00000332512.7:c.2034C>A ENSP00000332454.3:p.Ala678=
ENST00000352483.3:c.2178C>A ENSP00000330161.2:p.Ala726=
NM_020639.2:c.2034C>A NP_065690.2:p.Ala678=
NM_020639.3:c.2034C>A MANE Select NP_065690.2:p.Ala678=
Search 100 bp 5'
Search 100 bp 3'