Canonical Allele Identifier: CA410322229
Gene: RIPK4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.43176708G>T (hg19) chr21:g.41756548G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.41756548G>T , CM000683.2:g.41756548G>T GRCh38
NC_000021.8:g.43176708G>T , CM000683.1:g.43176708G>T GRCh37
NC_000021.7:g.42049777G>T NCBI36
NG_032113.1:g.15542C>A
NG_032113.2:g.15542C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000332512.8:c.451C>A MANE Select ENSP00000332454.3:p.Leu151Met
ENST00000332512.7:c.451C>A ENSP00000332454.3:p.Leu151Met
ENST00000352483.3:c.451C>A ENSP00000330161.2:p.Leu151Met
NM_020639.2:c.451C>A NP_065690.2:p.Leu151Met
NM_020639.3:c.451C>A MANE Select NP_065690.2:p.Leu151Met
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