Canonical Allele Identifier: CA364657807
Gene: BCKDHB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.80168933G>T , CM000668.2:g.80168933G>T GRCh38
NC_000006.11:g.80878650G>T , CM000668.1:g.80878650G>T GRCh37
NC_000006.10:g.80935369G>T NCBI36
NG_009775.1:g.67307G>T
NG_009775.2:g.67307G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000320393.9:c.536G>T MANE Select ENSP00000318351.5:p.Ser179Ile
ENST00000320393.8:c.536G>T ENSP00000318351.5:p.Ser179Ile
ENST00000356489.9:c.536G>T ENSP00000348880.5:p.Ser179Ile
ENST00000369760.8:c.536G>T ENSP00000358775.4:p.Ser179Ile
NM_000056.3:c.536G>T NP_000047.1:p.Ser179Ile
NM_183050.2:c.536G>T NP_898871.1:p.Ser179Ile
XM_005248756.3:c.536G>T XP_005248813.1:p.Ser179Ile
XM_006715542.2:c.326G>T XP_006715605.1:p.Ser109Ile
XM_011536023.1:c.536G>T XP_011534325.1:p.Ser179Ile
XM_011536024.1:c.536G>T XP_011534326.1:p.Ser179Ile
XM_011536025.1:c.536G>T XP_011534327.1:p.Ser179Ile
XM_011536026.1:c.326G>T XP_011534328.1:p.Ser109Ile
XM_011536027.1:c.536G>T XP_011534329.1:p.Ser179Ile
NM_000056.4:c.536G>T NP_000047.1:p.Ser179Ile
NM_001318975.1:c.326G>T NP_001305904.1:p.Ser109Ile
NM_183050.3:c.536G>T NP_898871.1:p.Ser179Ile
NR_134945.1:n.620G>T
XM_005248756.5:c.536G>T XP_005248813.1:p.Ser179Ile
XM_011536023.3:c.536G>T XP_011534325.1:p.Ser179Ile
XM_011536024.3:c.536G>T XP_011534326.1:p.Ser179Ile
XM_011536025.3:c.536G>T XP_011534327.1:p.Ser179Ile
XR_001743546.2:n.566G>T
XR_001743547.2:n.566G>T
XR_001743548.2:n.566G>T
XR_001743549.2:n.566G>T
XR_002956292.1:n.566G>T
NM_183050.4:c.536G>T MANE Select NP_898871.1:p.Ser179Ile
NR_134945.2:n.559G>T
NM_000056.5:c.536G>T NP_000047.1:p.Ser179Ile