Canonical Allele Identifier: CA1090990721
Gene: BCKDHB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.80168440_80168490del , CM000668.2:g.80168440_80168490del GRCh38
NC_000006.11:g.80878157_80878207del , CM000668.1:g.80878157_80878207del GRCh37
NC_000006.10:g.80934876_80934926del NCBI36
NG_009775.1:g.66814_66864del
NG_009775.2:g.66814_66864del

Transcript Alleles

HGVS Amino-acid Change
ENST00000320393.9:c.478-435_478-385del MANE Select ENSP00000318351.5:n.478-435_478-385del
ENST00000320393.8:c.478-435_478-385del ENSP00000318351.5:n.478-435_478-385del
ENST00000356489.9:c.478-435_478-385del ENSP00000348880.5:n.478-435_478-385del
ENST00000369760.8:c.478-435_478-385del ENSP00000358775.4:n.478-435_478-385del
NM_000056.3:c.478-435_478-385del NP_000047.1:n.478-435_478-385del
NM_183050.2:c.478-435_478-385del NP_898871.1:n.478-435_478-385del
XM_005248756.3:c.478-435_478-385del XP_005248813.1:n.478-435_478-385del
XM_006715542.2:c.268-435_268-385del XP_006715605.1:n.268-435_268-385del
XM_011536023.1:c.478-435_478-385del XP_011534325.1:n.478-435_478-385del
XM_011536024.1:c.478-435_478-385del XP_011534326.1:n.478-435_478-385del
XM_011536025.1:c.478-435_478-385del XP_011534327.1:n.478-435_478-385del
XM_011536026.1:c.268-435_268-385del XP_011534328.1:n.268-435_268-385del
XM_011536027.1:c.478-435_478-385del XP_011534329.1:n.478-435_478-385del
NM_000056.4:c.478-435_478-385del NP_000047.1:n.478-435_478-385del
NM_001318975.1:c.268-435_268-385del NP_001305904.1:n.268-435_268-385del
NM_183050.3:c.478-435_478-385del NP_898871.1:n.478-435_478-385del
NR_134945.1:n.562-435_562-385del
XM_005248756.5:c.478-435_478-385del XP_005248813.1:n.478-435_478-385del
XM_011536023.3:c.478-435_478-385del XP_011534325.1:n.478-435_478-385del
XM_011536024.3:c.478-435_478-385del XP_011534326.1:n.478-435_478-385del
XM_011536025.3:c.478-435_478-385del XP_011534327.1:n.478-435_478-385del
XR_001743546.2:n.508-435_508-385del
XR_001743547.2:n.508-435_508-385del
XR_001743548.2:n.508-435_508-385del
XR_001743549.2:n.508-435_508-385del
XR_002956292.1:n.508-435_508-385del
NM_183050.4:c.478-435_478-385del MANE Select NP_898871.1:n.478-435_478-385del
NR_134945.2:n.501-435_501-385del
NM_000056.5:c.478-435_478-385del NP_000047.1:n.478-435_478-385del