Canonical Allele Identifier: CA917790324
Gene: BCKDHB HGNC NCBI

Linked Data

dbSNP Id: rs1582600734

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.80343773dup , CM000668.2:g.80343773dup GRCh38
NC_000006.11:g.81053490dup , CM000668.1:g.81053490dup GRCh37
NC_000006.10:g.81110209dup NCBI36
NG_009775.1:g.242147dup
NG_009775.2:g.242147dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000320393.9:c.1148dup MANE Select ENSP00000318351.5:p.Tyr383Ter
ENST00000320393.8:c.1148dup ENSP00000318351.5:p.Tyr383Ter
ENST00000356489.9:c.1148dup ENSP00000348880.5:p.Tyr383Ter
ENST00000491328.1:n.203dup
NM_000056.3:c.1148dup NP_000047.1:p.Tyr383Ter
NM_183050.2:c.1148dup NP_898871.1:p.Tyr383Ter
XM_006715542.2:c.938dup XP_006715605.1:p.Tyr313Ter
XM_011536024.1:c.*154dup XP_011534326.1:n.*154dup
XM_011536026.1:c.938dup XP_011534328.1:p.Tyr313Ter
NM_000056.4:c.1148dup NP_000047.1:p.Tyr383Ter
NM_001318975.1:c.938dup NP_001305904.1:p.Tyr313Ter
NM_183050.3:c.1148dup NP_898871.1:p.Tyr383Ter
NR_134945.1:n.1326dup
XM_011536024.3:c.*154dup XP_011534326.1:n.*154dup
XR_001743546.2:n.1068+70552dup
XR_001743547.2:n.1068+70552dup
XR_001743548.2:n.1068+70552dup
XR_001743549.2:n.1068+70552dup
XR_002956292.1:n.1068+70552dup
NM_183050.4:c.1148dup MANE Select NP_898871.1:p.Tyr383Ter
NR_134945.2:n.1265dup
NM_000056.5:c.1148dup NP_000047.1:p.Tyr383Ter