Canonical Allele Identifier: CA512662906
Gene: RIPK4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.43161322A>G (hg19)
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Genomic Alleles

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

Transcript Alleles

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