Canonical Allele Identifier: CA2499214074

Gene: DBT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100206311_100206312delinsTT , CM000663.2:g.100206311_100206312delinsTT	GRCh38
NC_000001.10:g.100671867_100671868delinsTT , CM000663.1:g.100671867_100671868delinsTT	GRCh37
NC_000001.9:g.100444455_100444456delinsTT	NCBI36
NG_011852.2:g.48542_48543delinsAA

Transcript Alleles

HGVS	Amino-acid Change
NM_001918.5:c.1210-11_1210-10delinsAA MANE Select	NP_001909.4:n.1210-11_1210-10delinsAA
ENST00000370132.8:c.1210-11_1210-10delinsAA MANE Select	ENSP00000359151.3:n.1210-11_1210-10delinsAA
NM_001399969.1:c.667-11_667-10delinsAA	NP_001386898.1:n.667-11_667-10delinsAA
NM_001399972.1:c.667-11_667-10delinsAA	NP_001386901.1:n.667-11_667-10delinsAA
NM_001918.3:c.1210-11_1210-10delinsAA	NP_001909.3:n.1210-11_1210-10delinsAA
NM_001918.4:c.1210-11_1210-10delinsAA	NP_001909.3:n.1210-11_1210-10delinsAA
NR_174363.1:n.1042-11_1042-10delinsAA
NR_174364.1:n.1224-11_1224-10delinsAA
NR_174365.1:n.1007-11_1007-10delinsAA
NR_174366.1:n.1309-11_1309-10delinsAA
ENST00000681617.1:c.1336-11_1336-10delinsAA	ENSP00000505544.1:n.1336-11_1336-10delinsAA
ENST00000681780.1:c.667-11_667-10delinsAA	ENSP00000505780.1:n.667-11_667-10delinsAA
XM_005270545.2:c.667-11_667-10delinsAA	XP_005270602.1:n.667-11_667-10delinsAA
XM_005270545.4:c.667-11_667-10delinsAA	XP_005270602.1:n.667-11_667-10delinsAA
XM_005270546.2:c.667-11_667-10delinsAA	XP_005270603.1:n.667-11_667-10delinsAA
XM_017000468.2:c.667-11_667-10delinsAA	XP_016855957.1:n.667-11_667-10delinsAA
XM_017000469.2:c.667-11_667-10delinsAA	XP_016855958.1:n.667-11_667-10delinsAA