Canonical Allele Identifier: CA1090990717
Gene: BCKDHB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.80168452_80168558del , CM000668.2:g.80168452_80168558del GRCh38
NC_000006.11:g.80878169_80878275del , CM000668.1:g.80878169_80878275del GRCh37
NC_000006.10:g.80934888_80934994del NCBI36
NG_009775.1:g.66826_66932del
NG_009775.2:g.66826_66932del

Transcript Alleles

HGVS Amino-acid Change
ENST00000320393.9:c.478-423_478-317del MANE Select ENSP00000318351.5:n.478-423_478-317del
ENST00000320393.8:c.478-423_478-317del ENSP00000318351.5:n.478-423_478-317del
ENST00000356489.9:c.478-423_478-317del ENSP00000348880.5:n.478-423_478-317del
ENST00000369760.8:c.478-423_478-317del ENSP00000358775.4:n.478-423_478-317del
NM_000056.3:c.478-423_478-317del NP_000047.1:n.478-423_478-317del
NM_183050.2:c.478-423_478-317del NP_898871.1:n.478-423_478-317del
XM_005248756.3:c.478-423_478-317del XP_005248813.1:n.478-423_478-317del
XM_006715542.2:c.268-423_268-317del XP_006715605.1:n.268-423_268-317del
XM_011536023.1:c.478-423_478-317del XP_011534325.1:n.478-423_478-317del
XM_011536024.1:c.478-423_478-317del XP_011534326.1:n.478-423_478-317del
XM_011536025.1:c.478-423_478-317del XP_011534327.1:n.478-423_478-317del
XM_011536026.1:c.268-423_268-317del XP_011534328.1:n.268-423_268-317del
XM_011536027.1:c.478-423_478-317del XP_011534329.1:n.478-423_478-317del
NM_000056.4:c.478-423_478-317del NP_000047.1:n.478-423_478-317del
NM_001318975.1:c.268-423_268-317del NP_001305904.1:n.268-423_268-317del
NM_183050.3:c.478-423_478-317del NP_898871.1:n.478-423_478-317del
NR_134945.1:n.562-423_562-317del
XM_005248756.5:c.478-423_478-317del XP_005248813.1:n.478-423_478-317del
XM_011536023.3:c.478-423_478-317del XP_011534325.1:n.478-423_478-317del
XM_011536024.3:c.478-423_478-317del XP_011534326.1:n.478-423_478-317del
XM_011536025.3:c.478-423_478-317del XP_011534327.1:n.478-423_478-317del
XR_001743546.2:n.508-423_508-317del
XR_001743547.2:n.508-423_508-317del
XR_001743548.2:n.508-423_508-317del
XR_001743549.2:n.508-423_508-317del
XR_002956292.1:n.508-423_508-317del
NM_183050.4:c.478-423_478-317del MANE Select NP_898871.1:n.478-423_478-317del
NR_134945.2:n.501-423_501-317del
NM_000056.5:c.478-423_478-317del NP_000047.1:n.478-423_478-317del