Canonical Allele Identifier: CA410326382
Gene: RIPK4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.43161486G>C (hg19) chr21:g.41741326G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.41741326G>C , CM000683.2:g.41741326G>C GRCh38
NC_000021.8:g.43161486G>C , CM000683.1:g.43161486G>C GRCh37
NC_000021.7:g.42034555G>C NCBI36
NG_032113.1:g.30764C>G
NG_032113.2:g.30764C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000332512.8:c.1867C>G MANE Select ENSP00000332454.3:p.Leu623Val
ENST00000332512.7:c.1867C>G ENSP00000332454.3:p.Leu623Val
ENST00000352483.3:c.2011C>G ENSP00000330161.2:p.Leu671Val
NM_020639.2:c.1867C>G NP_065690.2:p.Leu623Val
NM_020639.3:c.1867C>G MANE Select NP_065690.2:p.Leu623Val
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