Canonical Allele Identifier: CA1184069682

Gene: DBT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100235373_100235375delinsAAT , CM000663.2:g.100235373_100235375delinsAAT	GRCh38
NC_000001.10:g.100700929_100700931delinsAAT , CM000663.1:g.100700929_100700931delinsAAT	GRCh37
NC_000001.9:g.100473517_100473519delinsAAT	NCBI36
NG_011852.2:g.19479_19481delinsATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681617.1:c.251+61_251+63delinsATT	ENSP00000505544.1:n.251+61_251+63delinsATT
ENST00000681780.1:c.-293+61_-293+63delinsATT	ENSP00000505780.1:n.-293+61_-293+63delinsATT
ENST00000370131.3:c.251+61_251+63delinsATT	ENSP00000359150.3:n.251+61_251+63delinsATT
ENST00000370132.8:c.251+61_251+63delinsATT MANE Select	ENSP00000359151.3:n.251+61_251+63delinsATT
NM_001918.3:c.251+61_251+63delinsATT	NP_001909.3:n.251+61_251+63delinsATT
XM_005270545.2:c.-293+61_-293+63delinsATT	XP_005270602.1:n.-293+61_-293+63delinsATT
XM_005270546.2:c.-111+61_-111+63delinsATT	XP_005270603.1:n.-111+61_-111+63delinsATT
XR_946560.1:n.271+61_271+63delinsATT
XM_005270545.4:c.-293+61_-293+63delinsATT	XP_005270602.1:n.-293+61_-293+63delinsATT
XM_017000468.2:c.-293+61_-293+63delinsATT	XP_016855957.1:n.-293+61_-293+63delinsATT
XM_017000469.2:c.-111+61_-111+63delinsATT	XP_016855958.1:n.-111+61_-111+63delinsATT
XR_946560.3:n.268+61_268+63delinsATT
NM_001918.4:c.251+61_251+63delinsATT	NP_001909.3:n.251+61_251+63delinsATT
NM_001918.5:c.251+61_251+63delinsATT MANE Select	NP_001909.4:n.251+61_251+63delinsATT
NM_001399969.1:c.-293+61_-293+63delinsATT	NP_001386898.1:n.-293+61_-293+63delinsATT
NM_001399972.1:c.-293+61_-293+63delinsATT	NP_001386901.1:n.-293+61_-293+63delinsATT
NR_174363.1:n.265+61_265+63delinsATT
NR_174364.1:n.265+61_265+63delinsATT
NR_174365.1:n.265+61_265+63delinsATT
NR_174366.1:n.265+61_265+63delinsATT