Canonical Allele Identifier: CA365021625
Gene: BCKDHB HGNC NCBI

Linked Data

gnomAD v4: 6-80343788-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.80343788A>G , CM000668.2:g.80343788A>G GRCh38
NC_000006.11:g.81053505A>G , CM000668.1:g.81053505A>G GRCh37
NC_000006.10:g.81110224A>G NCBI36
NG_009775.1:g.242162A>G
NG_009775.2:g.242162A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000320393.9:c.1163A>G MANE Select ENSP00000318351.5:p.Lys388Arg
ENST00000320393.8:c.1163A>G ENSP00000318351.5:p.Lys388Arg
ENST00000356489.9:c.1163A>G ENSP00000348880.5:p.Lys388Arg
ENST00000491328.1:n.218A>G
NM_000056.3:c.1163A>G NP_000047.1:p.Lys388Arg
NM_183050.2:c.1163A>G NP_898871.1:p.Lys388Arg
XM_006715542.2:c.953A>G XP_006715605.1:p.Lys318Arg
XM_011536024.1:c.*169A>G XP_011534326.1:n.*169A>G
XM_011536026.1:c.953A>G XP_011534328.1:p.Lys318Arg
NM_000056.4:c.1163A>G NP_000047.1:p.Lys388Arg
NM_001318975.1:c.953A>G NP_001305904.1:p.Lys318Arg
NM_183050.3:c.1163A>G NP_898871.1:p.Lys388Arg
NR_134945.1:n.1341A>G
XM_011536024.3:c.*169A>G XP_011534326.1:n.*169A>G
XR_001743546.2:n.1068+70567A>G
XR_001743547.2:n.1068+70567A>G
XR_001743548.2:n.1068+70567A>G
XR_001743549.2:n.1068+70567A>G
XR_002956292.1:n.1068+70567A>G
NM_183050.4:c.1163A>G MANE Select NP_898871.1:p.Lys388Arg
NR_134945.2:n.1280A>G
NM_000056.5:c.1163A>G NP_000047.1:p.Lys388Arg