Canonical Allele Identifier: CA129299
Gene: RIPK4 HGNC NCBI

Linked Data

ClinVar Variation Id: 30513
ClinVar RCV Id: RCV000023470
dbSNP Id: rs387906923

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.41756637A>T , CM000683.2:g.41756637A>T GRCh38
NC_000021.8:g.43176797A>T , CM000683.1:g.43176797A>T GRCh37
NC_000021.7:g.42049866A>T NCBI36
NG_032113.1:g.15453T>A
NG_032113.2:g.15453T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000332512.8:c.362T>A MANE Select ENSP00000332454.3:p.Ile121Asn
ENST00000332512.7:c.362T>A ENSP00000332454.3:p.Ile121Asn
ENST00000352483.3:c.362T>A ENSP00000330161.2:p.Ile121Asn
NM_020639.2:c.362T>A NP_065690.2:p.Ile121Asn
NM_020639.3:c.362T>A MANE Select NP_065690.2:p.Ile121Asn