Canonical Allele Identifier: CA1090990464
Gene: BCKDHB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.80168423_80168424insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA , CM000668.2:g.80168423_80168424insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA GRCh38
NC_000006.11:g.80878140_80878141insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA , CM000668.1:g.80878140_80878141insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA GRCh37
NC_000006.10:g.80934859_80934860insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA NCBI36
NG_009775.1:g.66797_66798insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA
NG_009775.2:g.66797_66798insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000320393.9:c.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA MANE Select ENSP00000318351.5:n.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAG...
ENST00000320393.8:c.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA ENSP00000318351.5:n.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAG...
ENST00000356489.9:c.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA ENSP00000348880.5:n.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAG...
ENST00000369760.8:c.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA ENSP00000358775.4:n.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAG...
NM_000056.3:c.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA NP_000047.1:n.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAGGGAGGG...
NM_183050.2:c.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA NP_898871.1:n.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAGGGAGGG...
XM_005248756.3:c.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA XP_005248813.1:n.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAGGGA...
XM_006715542.2:c.268-452_268-451insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA XP_006715605.1:n.268-452_268-451insGGGAAGGAAGAAAAGGATGAGAGGGA...
XM_011536023.1:c.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA XP_011534325.1:n.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAGGGA...
XM_011536024.1:c.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA XP_011534326.1:n.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAGGGA...
XM_011536025.1:c.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA XP_011534327.1:n.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAGGGA...
XM_011536026.1:c.268-452_268-451insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA XP_011534328.1:n.268-452_268-451insGGGAAGGAAGAAAAGGATGAGAGGGA...
XM_011536027.1:c.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA XP_011534329.1:n.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAGGGA...
NM_000056.4:c.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA NP_000047.1:n.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAGGGAGGG...
NM_001318975.1:c.268-452_268-451insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA NP_001305904.1:n.268-452_268-451insGGGAAGGAAGAAAAGGATGAGAGGGA...
NM_183050.3:c.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA NP_898871.1:n.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAGGGAGGG...
NR_134945.1:n.562-452_562-451insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA
XM_005248756.5:c.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA XP_005248813.1:n.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAGGGA...
XM_011536023.3:c.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA XP_011534325.1:n.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAGGGA...
XM_011536024.3:c.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA XP_011534326.1:n.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAGGGA...
XM_011536025.3:c.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA XP_011534327.1:n.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAGGGA...
XR_001743546.2:n.508-452_508-451insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA
XR_001743547.2:n.508-452_508-451insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA
XR_001743548.2:n.508-452_508-451insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA
XR_001743549.2:n.508-452_508-451insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA
XR_002956292.1:n.508-452_508-451insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA
NM_183050.4:c.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA MANE Select NP_898871.1:n.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAGGGAGGG...
NR_134945.2:n.501-452_501-451insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA
NM_000056.5:c.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAGGGAGGGAGGGAGGGAGGGA NP_000047.1:n.478-452_478-451insGGGAAGGAAGAAAAGGATGAGAGGGAGGG...