Canonical Allele Identifier: CA8021430
Gene: BCKDK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31109261G>C , CM000678.2:g.31109261G>C GRCh38
NC_000016.9:g.31120582G>C , CM000678.1:g.31120582G>C GRCh37
NC_000016.8:g.31028083G>C NCBI36
NG_033011.1:g.5968G>C

Transcript Alleles

HGVS Amino-acid Change
NM_005881.4:c.38G>C MANE Select NP_005872.2:p.Gly13Ala
ENST00000219794.11:c.38G>C MANE Select ENSP00000219794.6:p.Gly13Ala
NM_001122957.2:c.38G>C NP_001116429.1:p.Gly13Ala
NM_001122957.3:c.38G>C NP_001116429.1:p.Gly13Ala
NM_001122957.4:c.38G>C NP_001116429.1:p.Gly13Ala
NM_001271926.1:c.38G>C NP_001258855.1:p.Gly13Ala
NM_001271926.2:c.38G>C NP_001258855.1:p.Gly13Ala
NM_001271926.3:c.38G>C NP_001258855.1:p.Gly13Ala
NM_005881.3:c.38G>C NP_005872.2:p.Gly13Ala
ENST00000219794.10:c.38G>C ENSP00000219794.6:p.Gly13Ala
ENST00000287507.7:c.38G>C ENSP00000287507.3:p.Gly13Ala
ENST00000394950.7:c.38G>C ENSP00000378404.3:p.Gly13Ala
ENST00000394951.5:c.38G>C ENSP00000378405.1:p.Gly13Ala
ENST00000484226.2:c.38G>C ENSP00000457226.1:p.Gly13Ala
ENST00000561755.1:c.38G>C ENSP00000455866.1:p.Gly13Ala
ENST00000566568.1:n.246G>C
ENST00000567530.5:c.38G>C ENSP00000456479.1:p.Gly13Ala
ENST00000567676.1:c.38G>C ENSP00000454947.1:p.Gly13Ala
XM_017022859.1:c.38G>C XP_016878348.1:p.Gly13Ala