Canonical Allele Identifier: CA1640984724
Community Standard Title: NM_183050.4(BCKDHB):c.974T= (p.Leu325=)
Gene: BCKDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.80273157T= , CM000668.2:g.80273157T= GRCh38
NC_000006.11:g.80982874T= , CM000668.1:g.80982874T= GRCh37
NC_000006.10:g.81039593T= NCBI36
NG_009775.1:g.171531T=
NG_009775.2:g.171531T=

Transcript Alleles

HGVS Amino-acid Change
NM_183050.4:c.974T= MANE Select NP_898871.1:p.Leu325=
ENST00000320393.9:c.974T= MANE Select ENSP00000318351.5:p.Leu325=
NM_000056.3:c.974T= NP_000047.1:p.Leu325=
NM_000056.4:c.974T= NP_000047.1:p.Leu325=
NM_000056.5:c.974T= NP_000047.1:p.Leu325=
NM_001318975.1:c.764T= NP_001305904.1:p.Leu255=
NM_183050.2:c.974T= NP_898871.1:p.Leu325=
NM_183050.3:c.974T= NP_898871.1:p.Leu325=
NR_134945.1:n.1152T=
NR_134945.2:n.1091T=
ENST00000320393.8:c.974T= ENSP00000318351.5:p.Leu325=
ENST00000356489.9:c.974T= ENSP00000348880.5:p.Leu325=
ENST00000468520.1:n.204T=
XM_005248756.3:c.974T= XP_005248813.1:p.Leu325=
XM_005248756.5:c.974T= XP_005248813.1:p.Leu325=
XM_006715542.2:c.764T= XP_006715605.1:p.Leu255=
XM_011536023.1:c.974T= XP_011534325.1:p.Leu325=
XM_011536023.3:c.974T= XP_011534325.1:p.Leu325=
XM_011536024.1:c.974T= XP_011534326.1:p.Leu325=
XM_011536024.3:c.974T= XP_011534326.1:p.Leu325=
XM_011536025.1:c.974T= XP_011534327.1:p.Leu325=
XM_011536025.3:c.974T= XP_011534327.1:p.Leu325=
XM_011536026.1:c.764T= XP_011534328.1:p.Leu255=
XR_001743546.2:n.1004T=
XR_001743547.2:n.1004T=
XR_001743548.2:n.1004T=
XR_001743549.2:n.1004T=
XR_002956292.1:n.1004T=