Canonical Allele Identifier: CA2679497845
Gene: BCKDHB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.80168759_80168832del , CM000668.2:g.80168759_80168832del GRCh38
NC_000006.11:g.80878476_80878549del , CM000668.1:g.80878476_80878549del GRCh37
NC_000006.10:g.80935195_80935268del NCBI36
NG_009775.1:g.67133_67206del
NG_009775.2:g.67133_67206del

Transcript Alleles

HGVS Amino-acid Change
ENST00000320393.9:c.478-116_478-43del MANE Select ENSP00000318351.5:n.478-116_478-43del
ENST00000320393.8:c.478-116_478-43del ENSP00000318351.5:n.478-116_478-43del
ENST00000356489.9:c.478-116_478-43del ENSP00000348880.5:n.478-116_478-43del
ENST00000369760.8:c.478-116_478-43del ENSP00000358775.4:n.478-116_478-43del
NM_000056.3:c.478-116_478-43del NP_000047.1:n.478-116_478-43del
NM_183050.2:c.478-116_478-43del NP_898871.1:n.478-116_478-43del
XM_005248756.3:c.478-116_478-43del XP_005248813.1:n.478-116_478-43del
XM_006715542.2:c.268-116_268-43del XP_006715605.1:n.268-116_268-43del
XM_011536023.1:c.478-116_478-43del XP_011534325.1:n.478-116_478-43del
XM_011536024.1:c.478-116_478-43del XP_011534326.1:n.478-116_478-43del
XM_011536025.1:c.478-116_478-43del XP_011534327.1:n.478-116_478-43del
XM_011536026.1:c.268-116_268-43del XP_011534328.1:n.268-116_268-43del
XM_011536027.1:c.478-116_478-43del XP_011534329.1:n.478-116_478-43del
NM_000056.4:c.478-116_478-43del NP_000047.1:n.478-116_478-43del
NM_001318975.1:c.268-116_268-43del NP_001305904.1:n.268-116_268-43del
NM_183050.3:c.478-116_478-43del NP_898871.1:n.478-116_478-43del
NR_134945.1:n.562-116_562-43del
XM_005248756.5:c.478-116_478-43del XP_005248813.1:n.478-116_478-43del
XM_011536023.3:c.478-116_478-43del XP_011534325.1:n.478-116_478-43del
XM_011536024.3:c.478-116_478-43del XP_011534326.1:n.478-116_478-43del
XM_011536025.3:c.478-116_478-43del XP_011534327.1:n.478-116_478-43del
XR_001743546.2:n.508-116_508-43del
XR_001743547.2:n.508-116_508-43del
XR_001743548.2:n.508-116_508-43del
XR_001743549.2:n.508-116_508-43del
XR_002956292.1:n.508-116_508-43del
NM_183050.4:c.478-116_478-43del MANE Select NP_898871.1:n.478-116_478-43del
NR_134945.2:n.501-116_501-43del
NM_000056.5:c.478-116_478-43del NP_000047.1:n.478-116_478-43del