Canonical Allele Identifier: CA1184062223

Gene: DBT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100214770_100214774delinsCAAAT , CM000663.2:g.100214770_100214774delinsCAAAT	GRCh38
NC_000001.10:g.100680326_100680330delinsCAAAT , CM000663.1:g.100680326_100680330delinsCAAAT	GRCh37
NC_000001.9:g.100452914_100452918delinsCAAAT	NCBI36
NG_011852.2:g.40080_40084delinsATTTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000681617.1:c.939+43_939+47delinsATTTG	ENSP00000505544.1:n.939+43_939+47delinsATTTG
ENST00000681780.1:c.396+43_396+47delinsATTTG	ENSP00000505780.1:n.396+43_396+47delinsATTTG
ENST00000370131.3:c.939+43_939+47delinsATTTG	ENSP00000359150.3:n.939+43_939+47delinsATTTG
ENST00000370132.8:c.939+43_939+47delinsATTTG MANE Select	ENSP00000359151.3:n.939+43_939+47delinsATTTG
NM_001918.3:c.939+43_939+47delinsATTTG	NP_001909.3:n.939+43_939+47delinsATTTG
XM_005270545.2:c.396+43_396+47delinsATTTG	XP_005270602.1:n.396+43_396+47delinsATTTG
XM_005270546.2:c.396+43_396+47delinsATTTG	XP_005270603.1:n.396+43_396+47delinsATTTG
XR_946560.1:n.959+43_959+47delinsATTTG
XM_005270545.4:c.396+43_396+47delinsATTTG	XP_005270602.1:n.396+43_396+47delinsATTTG
XM_017000468.2:c.396+43_396+47delinsATTTG	XP_016855957.1:n.396+43_396+47delinsATTTG
XM_017000469.2:c.396+43_396+47delinsATTTG	XP_016855958.1:n.396+43_396+47delinsATTTG
XR_946560.3:n.956+43_956+47delinsATTTG
NM_001918.4:c.939+43_939+47delinsATTTG	NP_001909.3:n.939+43_939+47delinsATTTG
NM_001918.5:c.939+43_939+47delinsATTTG MANE Select	NP_001909.4:n.939+43_939+47delinsATTTG
NM_001399969.1:c.396+43_396+47delinsATTTG	NP_001386898.1:n.396+43_396+47delinsATTTG
NM_001399972.1:c.396+43_396+47delinsATTTG	NP_001386901.1:n.396+43_396+47delinsATTTG
NR_174363.1:n.771+43_771+47delinsATTTG
NR_174364.1:n.953+43_953+47delinsATTTG
NR_174365.1:n.736+43_736+47delinsATTTG
NR_174366.1:n.953+43_953+47delinsATTTG