Canonical Allele Identifier: CA512662867
Gene: RIPK4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.43161295G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.41741135G>C , CM000683.2:g.41741135G>C GRCh38
NC_000021.8:g.43161295G>C , CM000683.1:g.43161295G>C GRCh37
NC_000021.7:g.42034364G>C NCBI36
NG_032113.1:g.30955C>G
NG_032113.2:g.30955C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000332512.8:c.2058C>G MANE Select ENSP00000332454.3:p.Val686=
ENST00000332512.7:c.2058C>G ENSP00000332454.3:p.Val686=
ENST00000352483.3:c.2202C>G ENSP00000330161.2:p.Val734=
NM_020639.2:c.2058C>G NP_065690.2:p.Val686=
NM_020639.3:c.2058C>G MANE Select NP_065690.2:p.Val686=