Canonical Allele Identifier: CA2679499418

Gene: BCKDHB

Linked Data

• gnomAD v4: 6-80343913-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.80343913A>G , CM000668.2:g.80343913A>G	GRCh38
NC_000006.11:g.81053630A>G , CM000668.1:g.81053630A>G	GRCh37
NC_000006.10:g.81110349A>G	NCBI36
NG_009775.1:g.242287A>G
NG_009775.2:g.242287A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320393.9:c.*109A>G MANE Select	ENSP00000318351.5:n.*109A>G
ENST00000320393.8:c.*109A>G	ENSP00000318351.5:n.*109A>G
ENST00000356489.9:c.*8+101A>G	ENSP00000348880.5:n.*8+101A>G
ENST00000491328.1:n.242+101A>G
NM_000056.3:c.*8+101A>G	NP_000047.1:n.*8+101A>G
NM_183050.2:c.*109A>G	NP_898871.1:n.*109A>G
NM_000056.4:c.*8+101A>G	NP_000047.1:n.*8+101A>G
NM_001318975.1:c.*109A>G	NP_001305904.1:n.*109A>G
NM_183050.3:c.*109A>G	NP_898871.1:n.*109A>G
NR_134945.1:n.1466A>G
XM_011536024.3:c.*294A>G	XP_011534326.1:n.*294A>G
XR_001743546.2:n.1068+70692A>G
XR_001743547.2:n.1068+70692A>G
XR_001743548.2:n.1068+70692A>G
XR_001743549.2:n.1068+70692A>G
XR_002956292.1:n.1068+70692A>G
NM_183050.4:c.*109A>G MANE Select	NP_898871.1:n.*109A>G
NR_134945.2:n.1405A>G
NM_000056.5:c.*8+101A>G	NP_000047.1:n.*8+101A>G