Canonical Allele Identifier: CA1184062220
Gene: DBT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100214766_100214767delinsCA , CM000663.2:g.100214766_100214767delinsCA GRCh38
NC_000001.10:g.100680322_100680323delinsCA , CM000663.1:g.100680322_100680323delinsCA GRCh37
NC_000001.9:g.100452910_100452911delinsCA NCBI36
NG_011852.2:g.40087_40088delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000681617.1:c.939+50_939+51delinsTG ENSP00000505544.1:n.939+50_939+51delinsTG...
ENST00000681780.1:c.396+50_396+51delinsTG ENSP00000505780.1:n.396+50_396+51delinsTG...
ENST00000370131.3:c.939+50_939+51delinsTG ENSP00000359150.3:n.939+50_939+51delinsTG...
ENST00000370132.8:c.939+50_939+51delinsTG MANE Select ENSP00000359151.3:n.939+50_939+51delinsTG...
NM_001918.3:c.939+50_939+51delinsTG NP_001909.3:n.939+50_939+51delinsTG
XM_005270545.2:c.396+50_396+51delinsTG XP_005270602.1:n.396+50_396+51delinsTG
XM_005270546.2:c.396+50_396+51delinsTG XP_005270603.1:n.396+50_396+51delinsTG
XR_946560.1:n.959+50_959+51delinsTG
XM_005270545.4:c.396+50_396+51delinsTG XP_005270602.1:n.396+50_396+51delinsTG
XM_017000468.2:c.396+50_396+51delinsTG XP_016855957.1:n.396+50_396+51delinsTG
XM_017000469.2:c.396+50_396+51delinsTG XP_016855958.1:n.396+50_396+51delinsTG
XR_946560.3:n.956+50_956+51delinsTG
NM_001918.4:c.939+50_939+51delinsTG NP_001909.3:n.939+50_939+51delinsTG
NM_001918.5:c.939+50_939+51delinsTG MANE Select NP_001909.4:n.939+50_939+51delinsTG
NM_001399969.1:c.396+50_396+51delinsTG NP_001386898.1:n.396+50_396+51delinsTG
NM_001399972.1:c.396+50_396+51delinsTG NP_001386901.1:n.396+50_396+51delinsTG
NR_174363.1:n.771+50_771+51delinsTG
NR_174364.1:n.953+50_953+51delinsTG
NR_174365.1:n.736+50_736+51delinsTG
NR_174366.1:n.953+50_953+51delinsTG