Canonical Allele Identifier: CA512663792
Gene: RIPK4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.43176733C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.41756573C>A , CM000683.2:g.41756573C>A GRCh38
NC_000021.8:g.43176733C>A , CM000683.1:g.43176733C>A GRCh37
NC_000021.7:g.42049802C>A NCBI36
NG_032113.1:g.15517G>T
NG_032113.2:g.15517G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000332512.8:c.426G>T MANE Select ENSP00000332454.3:p.Leu142=
ENST00000332512.7:c.426G>T ENSP00000332454.3:p.Leu142=
ENST00000352483.3:c.426G>T ENSP00000330161.2:p.Leu142=
NM_020639.2:c.426G>T NP_065690.2:p.Leu142=
NM_020639.3:c.426G>T MANE Select NP_065690.2:p.Leu142=