Canonical Allele Identifier: CA1184062161

Gene: DBT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100214620G= , CM000663.2:g.100214620G=	GRCh38
NC_000001.10:g.100680176G= , CM000663.1:g.100680176G=	GRCh37
NC_000001.9:g.100452764G=	NCBI36
NG_011852.2:g.40234C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681617.1:c.939+197C=	ENSP00000505544.1:n.939+197C=
ENST00000681780.1:c.396+197C=	ENSP00000505780.1:n.396+197C=
ENST00000370131.3:c.939+197C=	ENSP00000359150.3:n.939+197C=
ENST00000370132.8:c.939+197C= MANE Select	ENSP00000359151.3:n.939+197C=
NM_001918.3:c.939+197C=	NP_001909.3:n.939+197C=
XM_005270545.2:c.396+197C=	XP_005270602.1:n.396+197C=
XM_005270546.2:c.396+197C=	XP_005270603.1:n.396+197C=
XR_946560.1:n.959+197C=
XM_005270545.4:c.396+197C=	XP_005270602.1:n.396+197C=
XM_017000468.2:c.396+197C=	XP_016855957.1:n.396+197C=
XM_017000469.2:c.396+197C=	XP_016855958.1:n.396+197C=
XR_946560.3:n.956+197C=
NM_001918.4:c.939+197C=	NP_001909.3:n.939+197C=
NM_001918.5:c.939+197C= MANE Select	NP_001909.4:n.939+197C=
NM_001399969.1:c.396+197C=	NP_001386898.1:n.396+197C=
NM_001399972.1:c.396+197C=	NP_001386901.1:n.396+197C=
NR_174363.1:n.771+197C=
NR_174364.1:n.953+197C=
NR_174365.1:n.736+197C=
NR_174366.1:n.953+197C=