Canonical Allele Identifier: CA1184062329
Gene: DBT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100215102_100215103delinsAC , CM000663.2:g.100215102_100215103delinsAC GRCh38
NC_000001.10:g.100680658_100680659delinsAC , CM000663.1:g.100680658_100680659delinsAC GRCh37
NC_000001.9:g.100453246_100453247delinsAC NCBI36
NG_011852.2:g.39751_39752delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000681617.1:c.773-120_773-119delinsGT ENSP00000505544.1:n.773-120_773-119delinsGT
ENST00000681780.1:c.230-120_230-119delinsGT ENSP00000505780.1:n.230-120_230-119delinsGT
ENST00000370131.3:c.773-120_773-119delinsGT ENSP00000359150.3:n.773-120_773-119delinsGT
ENST00000370132.8:c.773-120_773-119delinsGT MANE Select ENSP00000359151.3:n.773-120_773-119delinsGT
NM_001918.3:c.773-120_773-119delinsGT NP_001909.3:n.773-120_773-119delinsGT
XM_005270545.2:c.230-120_230-119delinsGT XP_005270602.1:n.230-120_230-119delinsGT
XM_005270546.2:c.230-120_230-119delinsGT XP_005270603.1:n.230-120_230-119delinsGT
XR_946560.1:n.793-120_793-119delinsGT
XM_005270545.4:c.230-120_230-119delinsGT XP_005270602.1:n.230-120_230-119delinsGT
XM_017000468.2:c.230-120_230-119delinsGT XP_016855957.1:n.230-120_230-119delinsGT
XM_017000469.2:c.230-120_230-119delinsGT XP_016855958.1:n.230-120_230-119delinsGT
XR_946560.3:n.790-120_790-119delinsGT
NM_001918.4:c.773-120_773-119delinsGT NP_001909.3:n.773-120_773-119delinsGT
NM_001918.5:c.773-120_773-119delinsGT MANE Select NP_001909.4:n.773-120_773-119delinsGT
NM_001399969.1:c.230-120_230-119delinsGT NP_001386898.1:n.230-120_230-119delinsGT
NM_001399972.1:c.230-120_230-119delinsGT NP_001386901.1:n.230-120_230-119delinsGT
NR_174363.1:n.605-120_605-119delinsGT
NR_174364.1:n.787-120_787-119delinsGT
NR_174365.1:n.570-120_570-119delinsGT
NR_174366.1:n.787-120_787-119delinsGT