Canonical Allele Identifier: CA512663066
Gene: RIPK4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.43161412C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.41741252C>A , CM000683.2:g.41741252C>A GRCh38
NC_000021.8:g.43161412C>A , CM000683.1:g.43161412C>A GRCh37
NC_000021.7:g.42034481C>A NCBI36
NG_032113.1:g.30838G>T
NG_032113.2:g.30838G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000332512.8:c.1941G>T MANE Select ENSP00000332454.3:p.Thr647=
ENST00000332512.7:c.1941G>T ENSP00000332454.3:p.Thr647=
ENST00000352483.3:c.2085G>T ENSP00000330161.2:p.Thr695=
NM_020639.2:c.1941G>T NP_065690.2:p.Thr647=
NM_020639.3:c.1941G>T MANE Select NP_065690.2:p.Thr647=
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