Canonical Allele Identifier: CA410325797
Gene: RIPK4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.43161313G>T (hg19) chr21:g.41741153G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.41741153G>T , CM000683.2:g.41741153G>T GRCh38
NC_000021.8:g.43161313G>T , CM000683.1:g.43161313G>T GRCh37
NC_000021.7:g.42034382G>T NCBI36
NG_032113.1:g.30937C>A
NG_032113.2:g.30937C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000332512.8:c.2040C>A MANE Select ENSP00000332454.3:p.Asn680Lys
ENST00000332512.7:c.2040C>A ENSP00000332454.3:p.Asn680Lys
ENST00000352483.3:c.2184C>A ENSP00000330161.2:p.Asn728Lys
NM_020639.2:c.2040C>A NP_065690.2:p.Asn680Lys
NM_020639.3:c.2040C>A MANE Select NP_065690.2:p.Asn680Lys
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