Canonical Allele Identifier: CA365021595
Gene: BCKDHB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.80343773A>T , CM000668.2:g.80343773A>T GRCh38
NC_000006.11:g.81053490A>T , CM000668.1:g.81053490A>T GRCh37
NC_000006.10:g.81110209A>T NCBI36
NG_009775.1:g.242147A>T
NG_009775.2:g.242147A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000320393.9:c.1148A>T MANE Select ENSP00000318351.5:p.Tyr383Phe
ENST00000320393.8:c.1148A>T ENSP00000318351.5:p.Tyr383Phe
ENST00000356489.9:c.1148A>T ENSP00000348880.5:p.Tyr383Phe
ENST00000491328.1:n.203A>T
NM_000056.3:c.1148A>T NP_000047.1:p.Tyr383Phe
NM_183050.2:c.1148A>T NP_898871.1:p.Tyr383Phe
XM_006715542.2:c.938A>T XP_006715605.1:p.Tyr313Phe
XM_011536024.1:c.*154A>T XP_011534326.1:n.*154A>T
XM_011536026.1:c.938A>T XP_011534328.1:p.Tyr313Phe
NM_000056.4:c.1148A>T NP_000047.1:p.Tyr383Phe
NM_001318975.1:c.938A>T NP_001305904.1:p.Tyr313Phe
NM_183050.3:c.1148A>T NP_898871.1:p.Tyr383Phe
NR_134945.1:n.1326A>T
XM_011536024.3:c.*154A>T XP_011534326.1:n.*154A>T
XR_001743546.2:n.1068+70552A>T
XR_001743547.2:n.1068+70552A>T
XR_001743548.2:n.1068+70552A>T
XR_001743549.2:n.1068+70552A>T
XR_002956292.1:n.1068+70552A>T
NM_183050.4:c.1148A>T MANE Select NP_898871.1:p.Tyr383Phe
NR_134945.2:n.1265A>T
NM_000056.5:c.1148A>T NP_000047.1:p.Tyr383Phe