Canonical Allele Identifier: CA2578677748

Gene: BCKDHB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.80168794_80168795insAAGGGAGGGAGGGG , CM000668.2:g.80168794_80168795insAAGGGAGGGAGGGG	GRCh38
NC_000006.11:g.80878511_80878512insAAGGGAGGGAGGGG , CM000668.1:g.80878511_80878512insAAGGGAGGGAGGGG	GRCh37
NC_000006.10:g.80935230_80935231insAAGGGAGGGAGGGG	NCBI36
NG_009775.1:g.67168_67169insAAGGGAGGGAGGGG
NG_009775.2:g.67168_67169insAAGGGAGGGAGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320393.9:c.478-81_478-80insAAGGGAGGGAGGGG MANE Select	ENSP00000318351.5:n.478-81_478-80insAAGGGAGGGAGGGG
ENST00000320393.8:c.478-81_478-80insAAGGGAGGGAGGGG	ENSP00000318351.5:n.478-81_478-80insAAGGGAGGGAGGGG
ENST00000356489.9:c.478-81_478-80insAAGGGAGGGAGGGG	ENSP00000348880.5:n.478-81_478-80insAAGGGAGGGAGGGG
ENST00000369760.8:c.478-81_478-80insAAGGGAGGGAGGGG	ENSP00000358775.4:n.478-81_478-80insAAGGGAGGGAGGGG
NM_000056.3:c.478-81_478-80insAAGGGAGGGAGGGG	NP_000047.1:n.478-81_478-80insAAGGGAGGGAGGGG
NM_183050.2:c.478-81_478-80insAAGGGAGGGAGGGG	NP_898871.1:n.478-81_478-80insAAGGGAGGGAGGGG
XM_005248756.3:c.478-81_478-80insAAGGGAGGGAGGGG	XP_005248813.1:n.478-81_478-80insAAGGGAGGGAGGGG
XM_006715542.2:c.268-81_268-80insAAGGGAGGGAGGGG	XP_006715605.1:n.268-81_268-80insAAGGGAGGGAGGGG
XM_011536023.1:c.478-81_478-80insAAGGGAGGGAGGGG	XP_011534325.1:n.478-81_478-80insAAGGGAGGGAGGGG
XM_011536024.1:c.478-81_478-80insAAGGGAGGGAGGGG	XP_011534326.1:n.478-81_478-80insAAGGGAGGGAGGGG
XM_011536025.1:c.478-81_478-80insAAGGGAGGGAGGGG	XP_011534327.1:n.478-81_478-80insAAGGGAGGGAGGGG
XM_011536026.1:c.268-81_268-80insAAGGGAGGGAGGGG	XP_011534328.1:n.268-81_268-80insAAGGGAGGGAGGGG
XM_011536027.1:c.478-81_478-80insAAGGGAGGGAGGGG	XP_011534329.1:n.478-81_478-80insAAGGGAGGGAGGGG
NM_000056.4:c.478-81_478-80insAAGGGAGGGAGGGG	NP_000047.1:n.478-81_478-80insAAGGGAGGGAGGGG
NM_001318975.1:c.268-81_268-80insAAGGGAGGGAGGGG	NP_001305904.1:n.268-81_268-80insAAGGGAGGGAGGGG
NM_183050.3:c.478-81_478-80insAAGGGAGGGAGGGG	NP_898871.1:n.478-81_478-80insAAGGGAGGGAGGGG
NR_134945.1:n.562-81_562-80insAAGGGAGGGAGGGG
XM_005248756.5:c.478-81_478-80insAAGGGAGGGAGGGG	XP_005248813.1:n.478-81_478-80insAAGGGAGGGAGGGG
XM_011536023.3:c.478-81_478-80insAAGGGAGGGAGGGG	XP_011534325.1:n.478-81_478-80insAAGGGAGGGAGGGG
XM_011536024.3:c.478-81_478-80insAAGGGAGGGAGGGG	XP_011534326.1:n.478-81_478-80insAAGGGAGGGAGGGG
XM_011536025.3:c.478-81_478-80insAAGGGAGGGAGGGG	XP_011534327.1:n.478-81_478-80insAAGGGAGGGAGGGG
XR_001743546.2:n.508-81_508-80insAAGGGAGGGAGGGG
XR_001743547.2:n.508-81_508-80insAAGGGAGGGAGGGG
XR_001743548.2:n.508-81_508-80insAAGGGAGGGAGGGG
XR_001743549.2:n.508-81_508-80insAAGGGAGGGAGGGG
XR_002956292.1:n.508-81_508-80insAAGGGAGGGAGGGG
NM_183050.4:c.478-81_478-80insAAGGGAGGGAGGGG MANE Select	NP_898871.1:n.478-81_478-80insAAGGGAGGGAGGGG
NR_134945.2:n.501-81_501-80insAAGGGAGGGAGGGG
NM_000056.5:c.478-81_478-80insAAGGGAGGGAGGGG	NP_000047.1:n.478-81_478-80insAAGGGAGGGAGGGG