Canonical Allele Identifier: CA451075152

Gene: BCKDHB

Linked Data

• MyVariant Identifiers: chr6:g.81053515C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.80343798C>T , CM000668.2:g.80343798C>T	GRCh38
NC_000006.11:g.81053515C>T , CM000668.1:g.81053515C>T	GRCh37
NC_000006.10:g.81110234C>T	NCBI36
NG_009775.1:g.242172C>T
NG_009775.2:g.242172C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320393.9:c.1173C>T MANE Select	ENSP00000318351.5:p.Asn391=
ENST00000320393.8:c.1173C>T	ENSP00000318351.5:p.Asn391=
ENST00000356489.9:c.1173C>T	ENSP00000348880.5:p.Asn391=
ENST00000491328.1:n.228C>T
NM_000056.3:c.1173C>T	NP_000047.1:p.Asn391=
NM_183050.2:c.1173C>T	NP_898871.1:p.Asn391=
XM_006715542.2:c.963C>T	XP_006715605.1:p.Asn321=
XM_011536024.1:c.*179C>T	XP_011534326.1:n.*179C>T
XM_011536026.1:c.963C>T	XP_011534328.1:p.Asn321=
NM_000056.4:c.1173C>T	NP_000047.1:p.Asn391=
NM_001318975.1:c.963C>T	NP_001305904.1:p.Asn321=
NM_183050.3:c.1173C>T	NP_898871.1:p.Asn391=
NR_134945.1:n.1351C>T
XM_011536024.3:c.*179C>T	XP_011534326.1:n.*179C>T
XR_001743546.2:n.1068+70577C>T
XR_001743547.2:n.1068+70577C>T
XR_001743548.2:n.1068+70577C>T
XR_001743549.2:n.1068+70577C>T
XR_002956292.1:n.1068+70577C>T
NM_183050.4:c.1173C>T MANE Select	NP_898871.1:p.Asn391=
NR_134945.2:n.1290C>T
NM_000056.5:c.1173C>T	NP_000047.1:p.Asn391=