Canonical Allele Identifier: CA512663209
Gene: RIPK4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.43161490G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.41741330G>T , CM000683.2:g.41741330G>T GRCh38
NC_000021.8:g.43161490G>T , CM000683.1:g.43161490G>T GRCh37
NC_000021.7:g.42034559G>T NCBI36
NG_032113.1:g.30760C>A
NG_032113.2:g.30760C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000332512.8:c.1863C>A MANE Select ENSP00000332454.3:p.Arg621=
ENST00000332512.7:c.1863C>A ENSP00000332454.3:p.Arg621=
ENST00000352483.3:c.2007C>A ENSP00000330161.2:p.Arg669=
NM_020639.2:c.1863C>A NP_065690.2:p.Arg621=
NM_020639.3:c.1863C>A MANE Select NP_065690.2:p.Arg621=