Canonical Allele Identifier: CA1145995553
Gene: DBT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100215103_100215105delinsCCC , CM000663.2:g.100215103_100215105delinsCCC GRCh38
NC_000001.10:g.100680659_100680661delinsCCC , CM000663.1:g.100680659_100680661delinsCCC GRCh37
NC_000001.9:g.100453247_100453249delinsCCC NCBI36
NG_011852.2:g.39749_39751delinsGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000681617.1:c.773-122_773-120delinsGGG ENSP00000505544.1:n.773-122_773-120delinsGGG
ENST00000681780.1:c.230-122_230-120delinsGGG ENSP00000505780.1:n.230-122_230-120delinsGGG
ENST00000370131.3:c.773-122_773-120delinsGGG ENSP00000359150.3:n.773-122_773-120delinsGGG
ENST00000370132.8:c.773-122_773-120delinsGGG MANE Select ENSP00000359151.3:n.773-122_773-120delinsGGG
NM_001918.3:c.773-122_773-120delinsGGG NP_001909.3:n.773-122_773-120delinsGGG
XM_005270545.2:c.230-122_230-120delinsGGG XP_005270602.1:n.230-122_230-120delinsGGG
XM_005270546.2:c.230-122_230-120delinsGGG XP_005270603.1:n.230-122_230-120delinsGGG
XR_946560.1:n.793-122_793-120delinsGGG
XM_005270545.4:c.230-122_230-120delinsGGG XP_005270602.1:n.230-122_230-120delinsGGG
XM_017000468.2:c.230-122_230-120delinsGGG XP_016855957.1:n.230-122_230-120delinsGGG
XM_017000469.2:c.230-122_230-120delinsGGG XP_016855958.1:n.230-122_230-120delinsGGG
XR_946560.3:n.790-122_790-120delinsGGG
NM_001918.4:c.773-122_773-120delinsGGG NP_001909.3:n.773-122_773-120delinsGGG
NM_001918.5:c.773-122_773-120delinsGGG MANE Select NP_001909.4:n.773-122_773-120delinsGGG
NM_001399969.1:c.230-122_230-120delinsGGG NP_001386898.1:n.230-122_230-120delinsGGG
NM_001399972.1:c.230-122_230-120delinsGGG NP_001386901.1:n.230-122_230-120delinsGGG
NR_174363.1:n.605-122_605-120delinsGGG
NR_174364.1:n.787-122_787-120delinsGGG
NR_174365.1:n.570-122_570-120delinsGGG
NR_174366.1:n.787-122_787-120delinsGGG