Canonical Allele Identifier: CA1184062333
Gene: DBT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100215105_100215106delinsCT , CM000663.2:g.100215105_100215106delinsCT GRCh38
NC_000001.10:g.100680661_100680662delinsCT , CM000663.1:g.100680661_100680662delinsCT GRCh37
NC_000001.9:g.100453249_100453250delinsCT NCBI36
NG_011852.2:g.39748_39749delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000681617.1:c.773-123_773-122delinsAG ENSP00000505544.1:n.773-123_773-122delinsAG
ENST00000681780.1:c.230-123_230-122delinsAG ENSP00000505780.1:n.230-123_230-122delinsAG
ENST00000370131.3:c.773-123_773-122delinsAG ENSP00000359150.3:n.773-123_773-122delinsAG
ENST00000370132.8:c.773-123_773-122delinsAG MANE Select ENSP00000359151.3:n.773-123_773-122delinsAG
NM_001918.3:c.773-123_773-122delinsAG NP_001909.3:n.773-123_773-122delinsAG
XM_005270545.2:c.230-123_230-122delinsAG XP_005270602.1:n.230-123_230-122delinsAG
XM_005270546.2:c.230-123_230-122delinsAG XP_005270603.1:n.230-123_230-122delinsAG
XR_946560.1:n.793-123_793-122delinsAG
XM_005270545.4:c.230-123_230-122delinsAG XP_005270602.1:n.230-123_230-122delinsAG
XM_017000468.2:c.230-123_230-122delinsAG XP_016855957.1:n.230-123_230-122delinsAG
XM_017000469.2:c.230-123_230-122delinsAG XP_016855958.1:n.230-123_230-122delinsAG
XR_946560.3:n.790-123_790-122delinsAG
NM_001918.4:c.773-123_773-122delinsAG NP_001909.3:n.773-123_773-122delinsAG
NM_001918.5:c.773-123_773-122delinsAG MANE Select NP_001909.4:n.773-123_773-122delinsAG
NM_001399969.1:c.230-123_230-122delinsAG NP_001386898.1:n.230-123_230-122delinsAG
NM_001399972.1:c.230-123_230-122delinsAG NP_001386901.1:n.230-123_230-122delinsAG
NR_174363.1:n.605-123_605-122delinsAG
NR_174364.1:n.787-123_787-122delinsAG
NR_174365.1:n.570-123_570-122delinsAG
NR_174366.1:n.787-123_787-122delinsAG