Canonical Allele Identifier: CA1640908623
Gene: BCKDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.80106696G= , CM000668.2:g.80106696G= GRCh38
NC_000006.11:g.80816413G= , CM000668.1:g.80816413G= GRCh37
NC_000006.10:g.80873132G= NCBI36
NG_009775.1:g.5070G=
NG_009775.2:g.5070G=

Transcript Alleles

HGVS Amino-acid change
ENST00000320393.9:c.3G= MANE Select ENSP00000318351.5:p.Met1=
ENST00000320393.8:c.3G= ENSP00000318351.5:p.Met1=
ENST00000356489.9:c.3G= ENSP00000348880.5:p.Met1=
ENST00000369760.8:c.3G= ENSP00000358775.4:p.Met1=
NM_000056.3:c.3G= NP_000047.1:p.Met1=
NM_183050.2:c.3G= NP_898871.1:p.Met1=
XM_005248756.3:c.3G= XP_005248813.1:p.Met1=
XM_006715542.2:c.-15+13G= XP_006715605.1:n.-15+13G=
XM_011536023.1:c.3G= XP_011534325.1:p.Met1=
XM_011536024.1:c.3G= XP_011534326.1:p.Met1=
XM_011536025.1:c.3G= XP_011534327.1:p.Met1=
XM_011536027.1:c.3G= XP_011534329.1:p.Met1=
NM_000056.4:c.3G= NP_000047.1:p.Met1=
NM_001318975.1:c.-15+13G= NP_001305904.1:n.-15+13G=
NM_183050.3:c.3G= NP_898871.1:p.Met1=
NR_134945.1:n.87G=
XM_005248756.5:c.3G= XP_005248813.1:p.Met1=
XM_011536023.3:c.3G= XP_011534325.1:p.Met1=
XM_011536024.3:c.3G= XP_011534326.1:p.Met1=
XM_011536025.3:c.3G= XP_011534327.1:p.Met1=
XR_001743546.2:n.33G=
XR_001743547.2:n.33G=
XR_001743548.2:n.33G=
XR_001743549.2:n.33G=
XR_002956292.1:n.33G=
NM_183050.4:c.3G= MANE Select NP_898871.1:p.Met1=
NR_134945.2:n.26G=
NM_000056.5:c.3G= NP_000047.1:p.Met1=