Canonical Allele Identifier: CA364660294

Gene: BCKDHB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.80203193A>T , CM000668.2:g.80203193A>T	GRCh38
NC_000006.11:g.80912910A>T , CM000668.1:g.80912910A>T	GRCh37
NC_000006.10:g.80969629A>T	NCBI36
NG_009775.1:g.101567A>T
NG_009775.2:g.101567A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_183050.4:c.932A>T MANE Select	NP_898871.1:p.Asp311Val
ENST00000320393.9:c.932A>T MANE Select	ENSP00000318351.5:p.Asp311Val
NM_000056.3:c.932A>T	NP_000047.1:p.Asp311Val
NM_000056.4:c.932A>T	NP_000047.1:p.Asp311Val
NM_000056.5:c.932A>T	NP_000047.1:p.Asp311Val
NM_001318975.1:c.722A>T	NP_001305904.1:p.Asp241Val
NM_183050.2:c.932A>T	NP_898871.1:p.Asp311Val
NM_183050.3:c.932A>T	NP_898871.1:p.Asp311Val
NR_134945.1:n.1110A>T
NR_134945.2:n.1049A>T
ENST00000320393.8:c.932A>T	ENSP00000318351.5:p.Asp311Val
ENST00000356489.9:c.932A>T	ENSP00000348880.5:p.Asp311Val
ENST00000468520.1:n.92A>T
XM_005248756.3:c.932A>T	XP_005248813.1:p.Asp311Val
XM_005248756.5:c.932A>T	XP_005248813.1:p.Asp311Val
XM_006715542.2:c.722A>T	XP_006715605.1:p.Asp241Val
XM_011536023.1:c.932A>T	XP_011534325.1:p.Asp311Val
XM_011536023.3:c.932A>T	XP_011534325.1:p.Asp311Val
XM_011536024.1:c.932A>T	XP_011534326.1:p.Asp311Val
XM_011536024.3:c.932A>T	XP_011534326.1:p.Asp311Val
XM_011536025.1:c.932A>T	XP_011534327.1:p.Asp311Val
XM_011536025.3:c.932A>T	XP_011534327.1:p.Asp311Val
XM_011536026.1:c.722A>T	XP_011534328.1:p.Asp241Val
XR_001743546.2:n.962A>T
XR_001743547.2:n.962A>T
XR_001743548.2:n.962A>T
XR_001743549.2:n.962A>T
XR_002956292.1:n.962A>T