Canonical Allele Identifier: CA749456787
Gene: RIPK4 HGNC NCBI

Linked Data

dbSNP Id: rs1432376776
gnomAD v3: 21-41756959-C-A
gnomAD v4: 21-41756959-C-A
MyVariant Identifiers: chr21:g.43177119C>A (hg19) chr21:g.41756959C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.41756959C>A , CM000683.2:g.41756959C>A GRCh38
NC_000021.8:g.43177119C>A , CM000683.1:g.43177119C>A GRCh37
NC_000021.7:g.42050188C>A NCBI36
NG_032113.1:g.15131G>T
NG_032113.2:g.15131G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000332512.8:c.183-143G>T MANE Select ENSP00000332454.3:n.183-143G>T
ENST00000332512.7:c.183-143G>T ENSP00000332454.3:n.183-143G>T
ENST00000352483.3:c.183-143G>T ENSP00000330161.2:n.183-143G>T
NM_020639.2:c.183-143G>T NP_065690.2:n.183-143G>T
NM_020639.3:c.183-143G>T MANE Select NP_065690.2:n.183-143G>T
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