Canonical Allele Identifier: CA2771864307

Gene: BCKDHB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.80168967_80168970del , CM000668.2:g.80168967_80168970del	GRCh38
NC_000006.11:g.80878684_80878687del , CM000668.1:g.80878684_80878687del	GRCh37
NC_000006.10:g.80935403_80935406del	NCBI36
NG_009775.1:g.67341_67344del
NG_009775.2:g.67341_67344del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320393.9:c.570_573del MANE Select	ENSP00000318351.5:p.His191GlyfsTer?
ENST00000320393.8:c.570_573del	ENSP00000318351.5:p.His191GlyfsTer?
ENST00000356489.9:c.570_573del	ENSP00000348880.5:p.His191GlyfsTer?
ENST00000369760.8:c.570_573del	ENSP00000358775.4:p.His191GlyfsTer24
NM_000056.3:c.570_573del	NP_000047.1:p.His191GlyfsTer?
NM_183050.2:c.570_573del	NP_898871.1:p.His191GlyfsTer?
XM_005248756.3:c.570_573del	XP_005248813.1:p.His191GlyfsTer?
XM_006715542.2:c.360_363del	XP_006715605.1:p.His121GlyfsTer?
XM_011536023.1:c.570_573del	XP_011534325.1:p.His191GlyfsTer?
XM_011536024.1:c.570_573del	XP_011534326.1:p.His191GlyfsTer?
XM_011536025.1:c.570_573del	XP_011534327.1:p.His191GlyfsTer?
XM_011536026.1:c.360_363del	XP_011534328.1:p.His121GlyfsTer?
XM_011536027.1:c.570_573del	XP_011534329.1:p.His191GlyfsTer24
NM_000056.4:c.570_573del	NP_000047.1:p.His191GlyfsTer?
NM_001318975.1:c.360_363del	NP_001305904.1:p.His121GlyfsTer?
NM_183050.3:c.570_573del	NP_898871.1:p.His191GlyfsTer?
NR_134945.1:n.654_657del
XM_005248756.5:c.570_573del	XP_005248813.1:p.His191GlyfsTer?
XM_011536023.3:c.570_573del	XP_011534325.1:p.His191GlyfsTer?
XM_011536024.3:c.570_573del	XP_011534326.1:p.His191GlyfsTer?
XM_011536025.3:c.570_573del	XP_011534327.1:p.His191GlyfsTer?
XR_001743546.2:n.600_603del
XR_001743547.2:n.600_603del
XR_001743548.2:n.600_603del
XR_001743549.2:n.600_603del
XR_002956292.1:n.600_603del
NM_183050.4:c.570_573del MANE Select	NP_898871.1:p.His191GlyfsTer?
NR_134945.2:n.593_596del
NM_000056.5:c.570_573del	NP_000047.1:p.His191GlyfsTer?