Canonical Allele Identifier: CA365021627
Gene: BCKDHB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.80343789A>C , CM000668.2:g.80343789A>C GRCh38
NC_000006.11:g.81053506A>C , CM000668.1:g.81053506A>C GRCh37
NC_000006.10:g.81110225A>C NCBI36
NG_009775.1:g.242163A>C
NG_009775.2:g.242163A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000320393.9:c.1164A>C MANE Select ENSP00000318351.5:p.Lys388Asn
ENST00000320393.8:c.1164A>C ENSP00000318351.5:p.Lys388Asn
ENST00000356489.9:c.1164A>C ENSP00000348880.5:p.Lys388Asn
ENST00000491328.1:n.219A>C
NM_000056.3:c.1164A>C NP_000047.1:p.Lys388Asn
NM_183050.2:c.1164A>C NP_898871.1:p.Lys388Asn
XM_006715542.2:c.954A>C XP_006715605.1:p.Lys318Asn
XM_011536024.1:c.*170A>C XP_011534326.1:n.*170A>C
XM_011536026.1:c.954A>C XP_011534328.1:p.Lys318Asn
NM_000056.4:c.1164A>C NP_000047.1:p.Lys388Asn
NM_001318975.1:c.954A>C NP_001305904.1:p.Lys318Asn
NM_183050.3:c.1164A>C NP_898871.1:p.Lys388Asn
NR_134945.1:n.1342A>C
XM_011536024.3:c.*170A>C XP_011534326.1:n.*170A>C
XR_001743546.2:n.1068+70568A>C
XR_001743547.2:n.1068+70568A>C
XR_001743548.2:n.1068+70568A>C
XR_001743549.2:n.1068+70568A>C
XR_002956292.1:n.1068+70568A>C
NM_183050.4:c.1164A>C MANE Select NP_898871.1:p.Lys388Asn
NR_134945.2:n.1281A>C
NM_000056.5:c.1164A>C NP_000047.1:p.Lys388Asn