Canonical Allele Identifier: CA451075153

Gene: BCKDHB

Linked Data

• MyVariant Identifiers: chr6:g.81053518T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.80343801T>C , CM000668.2:g.80343801T>C	GRCh38
NC_000006.11:g.81053518T>C , CM000668.1:g.81053518T>C	GRCh37
NC_000006.10:g.81110237T>C	NCBI36
NG_009775.1:g.242175T>C
NG_009775.2:g.242175T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320393.9:c.1176T>C MANE Select	ENSP00000318351.5:p.Tyr392=
ENST00000320393.8:c.1176T>C	ENSP00000318351.5:p.Tyr392=
ENST00000356489.9:c.1176T>C	ENSP00000348880.5:p.Tyr392=
ENST00000491328.1:n.231T>C
NM_000056.3:c.1176T>C	NP_000047.1:p.Tyr392=
NM_183050.2:c.1176T>C	NP_898871.1:p.Tyr392=
XM_006715542.2:c.966T>C	XP_006715605.1:p.Tyr322=
XM_011536024.1:c.*182T>C	XP_011534326.1:n.*182T>C
XM_011536026.1:c.966T>C	XP_011534328.1:p.Tyr322=
NM_000056.4:c.1176T>C	NP_000047.1:p.Tyr392=
NM_001318975.1:c.966T>C	NP_001305904.1:p.Tyr322=
NM_183050.3:c.1176T>C	NP_898871.1:p.Tyr392=
NR_134945.1:n.1354T>C
XM_011536024.3:c.*182T>C	XP_011534326.1:n.*182T>C
XR_001743546.2:n.1068+70580T>C
XR_001743547.2:n.1068+70580T>C
XR_001743548.2:n.1068+70580T>C
XR_001743549.2:n.1068+70580T>C
XR_002956292.1:n.1068+70580T>C
NM_183050.4:c.1176T>C MANE Select	NP_898871.1:p.Tyr392=
NR_134945.2:n.1293T>C
NM_000056.5:c.1176T>C	NP_000047.1:p.Tyr392=