Canonical Allele Identifier: CA512662904
Gene: RIPK4 HGNC NCBI

Linked Data

gnomAD v4: 21-41741162-A-C
MyVariant Identifiers: chr21:g.43161322A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.41741162A>C , CM000683.2:g.41741162A>C GRCh38
NC_000021.8:g.43161322A>C , CM000683.1:g.43161322A>C GRCh37
NC_000021.7:g.42034391A>C NCBI36
NG_032113.1:g.30928T>G
NG_032113.2:g.30928T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000332512.8:c.2031T>G MANE Select ENSP00000332454.3:p.Ala677=
ENST00000332512.7:c.2031T>G ENSP00000332454.3:p.Ala677=
ENST00000352483.3:c.2175T>G ENSP00000330161.2:p.Ala725=
NM_020639.2:c.2031T>G NP_065690.2:p.Ala677=
NM_020639.3:c.2031T>G MANE Select NP_065690.2:p.Ala677=
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