Canonical Allele Identifier: CA1640938797
Gene: BCKDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.80171116_80171120delinsTTATA , CM000668.2:g.80171116_80171120delinsTTATA GRCh38
NC_000006.11:g.80880833_80880837delinsTTATA , CM000668.1:g.80880833_80880837delinsTTATA GRCh37
NC_000006.10:g.80937552_80937556delinsTTATA NCBI36
NG_009775.1:g.69490_69494delinsTTATA
NG_009775.2:g.69490_69494delinsTTATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000320393.9:c.634-166_634-162delinsTTATA MANE Select ENSP00000318351.5:n.634-166_634-162delinsTTATA
ENST00000320393.8:c.634-166_634-162delinsTTATA ENSP00000318351.5:n.634-166_634-162delinsTTATA
ENST00000356489.9:c.634-166_634-162delinsTTATA ENSP00000348880.5:n.634-166_634-162delinsTTATA
NM_000056.3:c.634-166_634-162delinsTTATA NP_000047.1:n.634-166_634-162delinsTTATA
NM_183050.2:c.634-166_634-162delinsTTATA NP_898871.1:n.634-166_634-162delinsTTATA
XM_005248756.3:c.634-166_634-162delinsTTATA XP_005248813.1:n.634-166_634-162delinsTTATA
XM_006715542.2:c.424-166_424-162delinsTTATA XP_006715605.1:n.424-166_424-162delinsTTATA
XM_011536023.1:c.634-166_634-162delinsTTATA XP_011534325.1:n.634-166_634-162delinsTTATA
XM_011536024.1:c.634-166_634-162delinsTTATA XP_011534326.1:n.634-166_634-162delinsTTATA
XM_011536025.1:c.634-166_634-162delinsTTATA XP_011534327.1:n.634-166_634-162delinsTTATA
XM_011536026.1:c.424-166_424-162delinsTTATA XP_011534328.1:n.424-166_424-162delinsTTATA
NM_000056.4:c.634-166_634-162delinsTTATA NP_000047.1:n.634-166_634-162delinsTTATA
NM_001318975.1:c.424-166_424-162delinsTTATA NP_001305904.1:n.424-166_424-162delinsTTATA
NM_183050.3:c.634-166_634-162delinsTTATA NP_898871.1:n.634-166_634-162delinsTTATA
NR_134945.1:n.812-166_812-162delinsTTATA
XM_005248756.5:c.634-166_634-162delinsTTATA XP_005248813.1:n.634-166_634-162delinsTTATA
XM_011536023.3:c.634-166_634-162delinsTTATA XP_011534325.1:n.634-166_634-162delinsTTATA
XM_011536024.3:c.634-166_634-162delinsTTATA XP_011534326.1:n.634-166_634-162delinsTTATA
XM_011536025.3:c.634-166_634-162delinsTTATA XP_011534327.1:n.634-166_634-162delinsTTATA
XR_001743546.2:n.664-166_664-162delinsTTATA
XR_001743547.2:n.664-166_664-162delinsTTATA
XR_001743548.2:n.664-166_664-162delinsTTATA
XR_001743549.2:n.664-166_664-162delinsTTATA
XR_002956292.1:n.664-166_664-162delinsTTATA
NM_183050.4:c.634-166_634-162delinsTTATA MANE Select NP_898871.1:n.634-166_634-162delinsTTATA
NR_134945.2:n.751-166_751-162delinsTTATA
NM_000056.5:c.634-166_634-162delinsTTATA NP_000047.1:n.634-166_634-162delinsTTATA