Canonical Allele Identifier: CA410322398
Gene: RIPK4 HGNC NCBI

Linked Data

dbSNP Id: rs2061204230

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.41756614T>C , CM000683.2:g.41756614T>C GRCh38
NC_000021.8:g.43176774T>C , CM000683.1:g.43176774T>C GRCh37
NC_000021.7:g.42049843T>C NCBI36
NG_032113.1:g.15476A>G
NG_032113.2:g.15476A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000332512.8:c.385A>G MANE Select ENSP00000332454.3:p.Met129Val
ENST00000332512.7:c.385A>G ENSP00000332454.3:p.Met129Val
ENST00000352483.3:c.385A>G ENSP00000330161.2:p.Met129Val
NM_020639.2:c.385A>G NP_065690.2:p.Met129Val
NM_020639.3:c.385A>G MANE Select NP_065690.2:p.Met129Val