Canonical Allele Identifier: CA341337483

Gene: DBT

Linked Data

• MyVariant Identifiers: chr1:g.100680455T>A (hg19) ; chr1:g.100214899T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100214899T>A , CM000663.2:g.100214899T>A	GRCh38
NC_000001.10:g.100680455T>A , CM000663.1:g.100680455T>A	GRCh37
NC_000001.9:g.100453043T>A	NCBI36
NG_011852.2:g.39955A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681617.1:c.857A>T	ENSP00000505544.1:p.Glu286Val
ENST00000681780.1:c.314A>T	ENSP00000505780.1:p.Glu105Val
ENST00000370131.3:c.857A>T	ENSP00000359150.3:p.Glu286Val
ENST00000370132.8:c.857A>T MANE Select	ENSP00000359151.3:p.Glu286Val
NM_001918.3:c.857A>T	NP_001909.3:p.Glu286Val
XM_005270545.2:c.314A>T	XP_005270602.1:p.Glu105Val
XM_005270546.2:c.314A>T	XP_005270603.1:p.Glu105Val
XR_946560.1:n.877A>T
XM_005270545.4:c.314A>T	XP_005270602.1:p.Glu105Val
XM_017000468.2:c.314A>T	XP_016855957.1:p.Glu105Val
XM_017000469.2:c.314A>T	XP_016855958.1:p.Glu105Val
XR_946560.3:n.874A>T
NM_001918.4:c.857A>T	NP_001909.3:p.Glu286Val
NM_001918.5:c.857A>T MANE Select	NP_001909.4:p.Glu286Val
NM_001399969.1:c.314A>T	NP_001386898.1:p.Glu105Val
NM_001399972.1:c.314A>T	NP_001386901.1:p.Glu105Val
NR_174363.1:n.689A>T
NR_174364.1:n.871A>T
NR_174365.1:n.654A>T
NR_174366.1:n.871A>T