Canonical Allele Identifier: CA10035756
Gene: RIPK4 HGNC NCBI

Linked Data

dbSNP Id: rs770483025

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.41756490T>C , CM000683.2:g.41756490T>C GRCh38
NC_000021.8:g.43176650T>C , CM000683.1:g.43176650T>C GRCh37
NC_000021.7:g.42049719T>C NCBI36
NG_032113.1:g.15600A>G
NG_032113.2:g.15600A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000332512.8:c.474+35A>G MANE Select ENSP00000332454.3:n.474+35A>G
ENST00000332512.7:c.474+35A>G ENSP00000332454.3:n.474+35A>G
ENST00000352483.3:c.474+35A>G ENSP00000330161.2:n.474+35A>G
NM_020639.2:c.474+35A>G NP_065690.2:n.474+35A>G
NM_020639.3:c.474+35A>G MANE Select NP_065690.2:n.474+35A>G