Canonical Allele Identifier: CA10035429
Gene: RIPK4 HGNC NCBI

Linked Data

ClinVar Variation Id: 261346
dbSNP Id: rs2277789

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.41744072C>A , CM000683.2:g.41744072C>A GRCh38
NC_000021.8:g.43164232C>A , CM000683.1:g.43164232C>A GRCh37
NC_000021.7:g.42037301C>A NCBI36
NG_032113.1:g.28018G>T
NG_032113.2:g.28018G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000332512.8:c.1005G>T MANE Select ENSP00000332454.3:p.Leu335=
ENST00000332512.7:c.1005G>T ENSP00000332454.3:p.Leu335=
ENST00000352483.3:c.1149G>T ENSP00000330161.2:p.Leu383=
NM_020639.2:c.1005G>T NP_065690.2:p.Leu335=
NM_020639.3:c.1005G>T MANE Select NP_065690.2:p.Leu335=