Canonical Allele Identifier: CA2535761761
Gene: DBT HGNC NCBI

Linked Data

dbSNP Id: rs2100797702

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100215035_100215036insA , CM000663.2:g.100215035_100215036insA GRCh38
NC_000001.10:g.100680591_100680592insA , CM000663.1:g.100680591_100680592insA GRCh37
NC_000001.9:g.100453179_100453180insA NCBI36
NG_011852.2:g.39818_39819insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000681617.1:c.773-53_773-52insT ENSP00000505544.1:n.773-53_773-52insT
ENST00000681780.1:c.230-53_230-52insT ENSP00000505780.1:n.230-53_230-52insT
ENST00000370131.3:c.773-53_773-52insT ENSP00000359150.3:n.773-53_773-52insT
ENST00000370132.8:c.773-53_773-52insT MANE Select ENSP00000359151.3:n.773-53_773-52insT
NM_001918.3:c.773-53_773-52insT NP_001909.3:n.773-53_773-52insT
XM_005270545.2:c.230-53_230-52insT XP_005270602.1:n.230-53_230-52insT
XM_005270546.2:c.230-53_230-52insT XP_005270603.1:n.230-53_230-52insT
XR_946560.1:n.793-53_793-52insT
XM_005270545.4:c.230-53_230-52insT XP_005270602.1:n.230-53_230-52insT
XM_017000468.2:c.230-53_230-52insT XP_016855957.1:n.230-53_230-52insT
XM_017000469.2:c.230-53_230-52insT XP_016855958.1:n.230-53_230-52insT
XR_946560.3:n.790-53_790-52insT
NM_001918.4:c.773-53_773-52insT NP_001909.3:n.773-53_773-52insT
NM_001918.5:c.773-53_773-52insT MANE Select NP_001909.4:n.773-53_773-52insT
NM_001399969.1:c.230-53_230-52insT NP_001386898.1:n.230-53_230-52insT
NM_001399972.1:c.230-53_230-52insT NP_001386901.1:n.230-53_230-52insT
NR_174363.1:n.605-53_605-52insT
NR_174364.1:n.787-53_787-52insT
NR_174365.1:n.570-53_570-52insT
NR_174366.1:n.787-53_787-52insT