Canonical Allele Identifier: CA1640908630

Gene: BCKDHB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.80106706_80106716delinsGCGGCGGCTGC , CM000668.2:g.80106706_80106716delinsGCGGCGGCTGC	GRCh38
NC_000006.11:g.80816423_80816433delinsGCGGCGGCTGC , CM000668.1:g.80816423_80816433delinsGCGGCGGCTGC	GRCh37
NC_000006.10:g.80873142_80873152delinsGCGGCGGCTGC	NCBI36
NG_009775.1:g.5080_5090delinsGCGGCGGCTGC
NG_009775.2:g.5080_5090delinsGCGGCGGCTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320393.9:c.13_23delinsGCGGCGGCTGC MANE Select	ENSP00000318351.5:p.Ala5=
ENST00000320393.8:c.13_23delinsGCGGCGGCTGC	ENSP00000318351.5:p.Ala5=
ENST00000356489.9:c.13_23delinsGCGGCGGCTGC	ENSP00000348880.5:p.Ala5=
ENST00000369760.8:c.13_23delinsGCGGCGGCTGC	ENSP00000358775.4:p.Ala5=
NM_000056.3:c.13_23delinsGCGGCGGCTGC	NP_000047.1:p.Ala5=
NM_183050.2:c.13_23delinsGCGGCGGCTGC	NP_898871.1:p.Ala5=
XM_005248756.3:c.13_23delinsGCGGCGGCTGC	XP_005248813.1:p.Ala5=
XM_006715542.2:c.-15+23_-15+33delinsGCGGCGGCTGC	XP_006715605.1:n.-15+23_-15+33delinsGCGGCGGCTGC
XM_011536023.1:c.13_23delinsGCGGCGGCTGC	XP_011534325.1:p.Ala5=
XM_011536024.1:c.13_23delinsGCGGCGGCTGC	XP_011534326.1:p.Ala5=
XM_011536025.1:c.13_23delinsGCGGCGGCTGC	XP_011534327.1:p.Ala5=
XM_011536027.1:c.13_23delinsGCGGCGGCTGC	XP_011534329.1:p.Ala5=
NM_000056.4:c.13_23delinsGCGGCGGCTGC	NP_000047.1:p.Ala5=
NM_001318975.1:c.-15+23_-15+33delinsGCGGCGGCTGC	NP_001305904.1:n.-15+23_-15+33delinsGCGGCGGCTGC
NM_183050.3:c.13_23delinsGCGGCGGCTGC	NP_898871.1:p.Ala5=
NR_134945.1:n.97_107delinsGCGGCGGCTGC
XM_005248756.5:c.13_23delinsGCGGCGGCTGC	XP_005248813.1:p.Ala5=
XM_011536023.3:c.13_23delinsGCGGCGGCTGC	XP_011534325.1:p.Ala5=
XM_011536024.3:c.13_23delinsGCGGCGGCTGC	XP_011534326.1:p.Ala5=
XM_011536025.3:c.13_23delinsGCGGCGGCTGC	XP_011534327.1:p.Ala5=
XR_001743546.2:n.43_53delinsGCGGCGGCTGC
XR_001743547.2:n.43_53delinsGCGGCGGCTGC
XR_001743548.2:n.43_53delinsGCGGCGGCTGC
XR_001743549.2:n.43_53delinsGCGGCGGCTGC
XR_002956292.1:n.43_53delinsGCGGCGGCTGC
NM_183050.4:c.13_23delinsGCGGCGGCTGC MANE Select	NP_898871.1:p.Ala5=
NR_134945.2:n.36_46delinsGCGGCGGCTGC
NM_000056.5:c.13_23delinsGCGGCGGCTGC	NP_000047.1:p.Ala5=