Canonical Allele Identifier: CA2679497974

Gene: BCKDHB

Linked Data

• gnomAD v4: 6-80168799-G-GAGGGAGGGAGGA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.80168806_80168807insGAGGAAGGGAGG , CM000668.2:g.80168806_80168807insGAGGAAGGGAGG	GRCh38
NC_000006.11:g.80878523_80878524insGAGGAAGGGAGG , CM000668.1:g.80878523_80878524insGAGGAAGGGAGG	GRCh37
NC_000006.10:g.80935242_80935243insGAGGAAGGGAGG	NCBI36
NG_009775.1:g.67180_67181insGAGGAAGGGAGG
NG_009775.2:g.67180_67181insGAGGAAGGGAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320393.9:c.478-69_478-68insGAGGAAGGGAGG MANE Select	ENSP00000318351.5:n.478-69_478-68insGAGGAAGGGAGG
ENST00000320393.8:c.478-69_478-68insGAGGAAGGGAGG	ENSP00000318351.5:n.478-69_478-68insGAGGAAGGGAGG
ENST00000356489.9:c.478-69_478-68insGAGGAAGGGAGG	ENSP00000348880.5:n.478-69_478-68insGAGGAAGGGAGG
ENST00000369760.8:c.478-69_478-68insGAGGAAGGGAGG	ENSP00000358775.4:n.478-69_478-68insGAGGAAGGGAGG
NM_000056.3:c.478-69_478-68insGAGGAAGGGAGG	NP_000047.1:n.478-69_478-68insGAGGAAGGGAGG
NM_183050.2:c.478-69_478-68insGAGGAAGGGAGG	NP_898871.1:n.478-69_478-68insGAGGAAGGGAGG
XM_005248756.3:c.478-69_478-68insGAGGAAGGGAGG	XP_005248813.1:n.478-69_478-68insGAGGAAGGGAGG
XM_006715542.2:c.268-69_268-68insGAGGAAGGGAGG	XP_006715605.1:n.268-69_268-68insGAGGAAGGGAGG
XM_011536023.1:c.478-69_478-68insGAGGAAGGGAGG	XP_011534325.1:n.478-69_478-68insGAGGAAGGGAGG
XM_011536024.1:c.478-69_478-68insGAGGAAGGGAGG	XP_011534326.1:n.478-69_478-68insGAGGAAGGGAGG
XM_011536025.1:c.478-69_478-68insGAGGAAGGGAGG	XP_011534327.1:n.478-69_478-68insGAGGAAGGGAGG
XM_011536026.1:c.268-69_268-68insGAGGAAGGGAGG	XP_011534328.1:n.268-69_268-68insGAGGAAGGGAGG
XM_011536027.1:c.478-69_478-68insGAGGAAGGGAGG	XP_011534329.1:n.478-69_478-68insGAGGAAGGGAGG
NM_000056.4:c.478-69_478-68insGAGGAAGGGAGG	NP_000047.1:n.478-69_478-68insGAGGAAGGGAGG
NM_001318975.1:c.268-69_268-68insGAGGAAGGGAGG	NP_001305904.1:n.268-69_268-68insGAGGAAGGGAGG
NM_183050.3:c.478-69_478-68insGAGGAAGGGAGG	NP_898871.1:n.478-69_478-68insGAGGAAGGGAGG
NR_134945.1:n.562-69_562-68insGAGGAAGGGAGG
XM_005248756.5:c.478-69_478-68insGAGGAAGGGAGG	XP_005248813.1:n.478-69_478-68insGAGGAAGGGAGG
XM_011536023.3:c.478-69_478-68insGAGGAAGGGAGG	XP_011534325.1:n.478-69_478-68insGAGGAAGGGAGG
XM_011536024.3:c.478-69_478-68insGAGGAAGGGAGG	XP_011534326.1:n.478-69_478-68insGAGGAAGGGAGG
XM_011536025.3:c.478-69_478-68insGAGGAAGGGAGG	XP_011534327.1:n.478-69_478-68insGAGGAAGGGAGG
XR_001743546.2:n.508-69_508-68insGAGGAAGGGAGG
XR_001743547.2:n.508-69_508-68insGAGGAAGGGAGG
XR_001743548.2:n.508-69_508-68insGAGGAAGGGAGG
XR_001743549.2:n.508-69_508-68insGAGGAAGGGAGG
XR_002956292.1:n.508-69_508-68insGAGGAAGGGAGG
NM_183050.4:c.478-69_478-68insGAGGAAGGGAGG MANE Select	NP_898871.1:n.478-69_478-68insGAGGAAGGGAGG
NR_134945.2:n.501-69_501-68insGAGGAAGGGAGG
NM_000056.5:c.478-69_478-68insGAGGAAGGGAGG	NP_000047.1:n.478-69_478-68insGAGGAAGGGAGG