Canonical Allele Identifier: CA10604237

Gene: BCKDK

Linked Data

• ClinVar Variation Id: 282610
• ClinVar RCV Id: RCV000317979
• dbSNP Id: rs397514573
• gnomAD v4: 16-31110247-C-G
• MyVariant Identifiers: chr16:g.31121568C>G (hg19) ; chr16:g.31110247C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31110247C>G , CM000678.2:g.31110247C>G	GRCh38
NC_000016.9:g.31121568C>G , CM000678.1:g.31121568C>G	GRCh37
NC_000016.8:g.31029069C>G	NCBI36
NG_033011.1:g.6954C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219794.11:c.466C>G MANE Select	ENSP00000219794.6:p.Arg156Gly
ENST00000219794.10:c.466C>G	ENSP00000219794.6:p.Arg156Gly
ENST00000287507.7:c.466C>G	ENSP00000287507.3:p.Arg156Gly
ENST00000394950.7:c.466C>G	ENSP00000378404.3:p.Arg156Gly
ENST00000394951.5:c.466C>G	ENSP00000378405.1:p.Arg156Gly
ENST00000484226.2:c.439C>G	ENSP00000457226.1:p.Arg147Gly
ENST00000566568.1:n.967C>G
ENST00000567530.5:c.466C>G	ENSP00000456479.1:p.Arg156Gly
NM_001122957.2:c.466C>G	NP_001116429.1:p.Arg156Gly
NM_001271926.1:c.466C>G	NP_001258855.1:p.Arg156Gly
NM_005881.3:c.466C>G	NP_005872.2:p.Arg156Gly
XM_017022859.1:c.466C>G	XP_016878348.1:p.Arg156Gly
NM_005881.4:c.466C>G MANE Select	NP_005872.2:p.Arg156Gly
NM_001122957.3:c.466C>G	NP_001116429.1:p.Arg156Gly
NM_001271926.2:c.466C>G	NP_001258855.1:p.Arg156Gly
NM_001122957.4:c.466C>G	NP_001116429.1:p.Arg156Gly
NM_001271926.3:c.466C>G	NP_001258855.1:p.Arg156Gly