Canonical Allele Identifier: CA1184058771

Gene: DBT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100206069_100206070delinsAG , CM000663.2:g.100206069_100206070delinsAG	GRCh38
NC_000001.10:g.100671625_100671626delinsAG , CM000663.1:g.100671625_100671626delinsAG	GRCh37
NC_000001.9:g.100444213_100444214delinsAG	NCBI36
NG_011852.2:g.48784_48785delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681617.1:c.1407+160_1407+161delinsCT	ENSP00000505544.1:n.1407+160_1407+161delinsCT
ENST00000681780.1:c.738+160_738+161delinsCT	ENSP00000505780.1:n.738+160_738+161delinsCT
ENST00000370132.8:c.1281+160_1281+161delinsCT MANE Select	ENSP00000359151.3:n.1281+160_1281+161delinsCT
NM_001918.3:c.1281+160_1281+161delinsCT	NP_001909.3:n.1281+160_1281+161delinsCT
XM_005270545.2:c.738+160_738+161delinsCT	XP_005270602.1:n.738+160_738+161delinsCT
XM_005270546.2:c.738+160_738+161delinsCT	XP_005270603.1:n.738+160_738+161delinsCT
XM_005270545.4:c.738+160_738+161delinsCT	XP_005270602.1:n.738+160_738+161delinsCT
XM_017000468.2:c.738+160_738+161delinsCT	XP_016855957.1:n.738+160_738+161delinsCT
XM_017000469.2:c.738+160_738+161delinsCT	XP_016855958.1:n.738+160_738+161delinsCT
NM_001918.4:c.1281+160_1281+161delinsCT	NP_001909.3:n.1281+160_1281+161delinsCT
NM_001918.5:c.1281+160_1281+161delinsCT MANE Select	NP_001909.4:n.1281+160_1281+161delinsCT
NM_001399969.1:c.738+160_738+161delinsCT	NP_001386898.1:n.738+160_738+161delinsCT
NM_001399972.1:c.738+160_738+161delinsCT	NP_001386901.1:n.738+160_738+161delinsCT
NR_174363.1:n.1113+160_1113+161delinsCT
NR_174364.1:n.1295+160_1295+161delinsCT
NR_174365.1:n.1078+160_1078+161delinsCT
NR_174366.1:n.1380+160_1380+161delinsCT