Canonical Allele Identifier: CA1640937793

Gene: BCKDHB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.80168974_80168976delinsGCT , CM000668.2:g.80168974_80168976delinsGCT	GRCh38
NC_000006.11:g.80878691_80878693delinsGCT , CM000668.1:g.80878691_80878693delinsGCT	GRCh37
NC_000006.10:g.80935410_80935412delinsGCT	NCBI36
NG_009775.1:g.67348_67350delinsGCT
NG_009775.2:g.67348_67350delinsGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320393.9:c.577_579delinsGCT MANE Select	ENSP00000318351.5:p.Ala193=
ENST00000320393.8:c.577_579delinsGCT	ENSP00000318351.5:p.Ala193=
ENST00000356489.9:c.577_579delinsGCT	ENSP00000348880.5:p.Ala193=
ENST00000369760.8:c.577_579delinsGCT	ENSP00000358775.4:p.Ala193=
NM_000056.3:c.577_579delinsGCT	NP_000047.1:p.Ala193=
NM_183050.2:c.577_579delinsGCT	NP_898871.1:p.Ala193=
XM_005248756.3:c.577_579delinsGCT	XP_005248813.1:p.Ala193=
XM_006715542.2:c.367_369delinsGCT	XP_006715605.1:p.Ala123=
XM_011536023.1:c.577_579delinsGCT	XP_011534325.1:p.Ala193=
XM_011536024.1:c.577_579delinsGCT	XP_011534326.1:p.Ala193=
XM_011536025.1:c.577_579delinsGCT	XP_011534327.1:p.Ala193=
XM_011536026.1:c.367_369delinsGCT	XP_011534328.1:p.Ala123=
XM_011536027.1:c.577_579delinsGCT	XP_011534329.1:p.Ala193=
NM_000056.4:c.577_579delinsGCT	NP_000047.1:p.Ala193=
NM_001318975.1:c.367_369delinsGCT	NP_001305904.1:p.Ala123=
NM_183050.3:c.577_579delinsGCT	NP_898871.1:p.Ala193=
NR_134945.1:n.661_663delinsGCT
XM_005248756.5:c.577_579delinsGCT	XP_005248813.1:p.Ala193=
XM_011536023.3:c.577_579delinsGCT	XP_011534325.1:p.Ala193=
XM_011536024.3:c.577_579delinsGCT	XP_011534326.1:p.Ala193=
XM_011536025.3:c.577_579delinsGCT	XP_011534327.1:p.Ala193=
XR_001743546.2:n.607_609delinsGCT
XR_001743547.2:n.607_609delinsGCT
XR_001743548.2:n.607_609delinsGCT
XR_001743549.2:n.607_609delinsGCT
XR_002956292.1:n.607_609delinsGCT
NM_183050.4:c.577_579delinsGCT MANE Select	NP_898871.1:p.Ala193=
NR_134945.2:n.600_602delinsGCT
NM_000056.5:c.577_579delinsGCT	NP_000047.1:p.Ala193=