Canonical Allele Identifier: CA512662855
Gene: RIPK4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.43161286A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.41741126A>T , CM000683.2:g.41741126A>T GRCh38
NC_000021.8:g.43161286A>T , CM000683.1:g.43161286A>T GRCh37
NC_000021.7:g.42034355A>T NCBI36
NG_032113.1:g.30964T>A
NG_032113.2:g.30964T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000332512.8:c.2067T>A MANE Select ENSP00000332454.3:p.Leu689=
ENST00000332512.7:c.2067T>A ENSP00000332454.3:p.Leu689=
ENST00000352483.3:c.2211T>A ENSP00000330161.2:p.Leu737=
NM_020639.2:c.2067T>A NP_065690.2:p.Leu689=
NM_020639.3:c.2067T>A MANE Select NP_065690.2:p.Leu689=