Canonical Allele Identifier: CA1640937799
Gene: BCKDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.80168988_80168990delinsTCA , CM000668.2:g.80168988_80168990delinsTCA GRCh38
NC_000006.11:g.80878705_80878707delinsTCA , CM000668.1:g.80878705_80878707delinsTCA GRCh37
NC_000006.10:g.80935424_80935426delinsTCA NCBI36
NG_009775.1:g.67362_67364delinsTCA
NG_009775.2:g.67362_67364delinsTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000320393.9:c.591_593delinsTCA MANE Select ENSP00000318351.5:p.Ser197=
ENST00000320393.8:c.591_593delinsTCA ENSP00000318351.5:p.Ser197=
ENST00000356489.9:c.591_593delinsTCA ENSP00000348880.5:p.Ser197=
ENST00000369760.8:c.591_593delinsTCA ENSP00000358775.4:p.Ser197=
NM_000056.3:c.591_593delinsTCA NP_000047.1:p.Ser197=
NM_183050.2:c.591_593delinsTCA NP_898871.1:p.Ser197=
XM_005248756.3:c.591_593delinsTCA XP_005248813.1:p.Ser197=
XM_006715542.2:c.381_383delinsTCA XP_006715605.1:p.Ser127=
XM_011536023.1:c.591_593delinsTCA XP_011534325.1:p.Ser197=
XM_011536024.1:c.591_593delinsTCA XP_011534326.1:p.Ser197=
XM_011536025.1:c.591_593delinsTCA XP_011534327.1:p.Ser197=
XM_011536026.1:c.381_383delinsTCA XP_011534328.1:p.Ser127=
XM_011536027.1:c.591_593delinsTCA XP_011534329.1:p.Ser197=
NM_000056.4:c.591_593delinsTCA NP_000047.1:p.Ser197=
NM_001318975.1:c.381_383delinsTCA NP_001305904.1:p.Ser127=
NM_183050.3:c.591_593delinsTCA NP_898871.1:p.Ser197=
NR_134945.1:n.675_677delinsTCA
XM_005248756.5:c.591_593delinsTCA XP_005248813.1:p.Ser197=
XM_011536023.3:c.591_593delinsTCA XP_011534325.1:p.Ser197=
XM_011536024.3:c.591_593delinsTCA XP_011534326.1:p.Ser197=
XM_011536025.3:c.591_593delinsTCA XP_011534327.1:p.Ser197=
XR_001743546.2:n.621_623delinsTCA
XR_001743547.2:n.621_623delinsTCA
XR_001743548.2:n.621_623delinsTCA
XR_001743549.2:n.621_623delinsTCA
XR_002956292.1:n.621_623delinsTCA
NM_183050.4:c.591_593delinsTCA MANE Select NP_898871.1:p.Ser197=
NR_134945.2:n.614_616delinsTCA
NM_000056.5:c.591_593delinsTCA NP_000047.1:p.Ser197=