Canonical Allele Identifier: CA419101429

Gene: DBT

Linked Data

• MyVariant Identifiers: chr1:g.100680505T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100214949T>A , CM000663.2:g.100214949T>A	GRCh38
NC_000001.10:g.100680505T>A , CM000663.1:g.100680505T>A	GRCh37
NC_000001.9:g.100453093T>A	NCBI36
NG_011852.2:g.39905A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681617.1:c.807A>T	ENSP00000505544.1:p.Ala269=
ENST00000681780.1:c.264A>T	ENSP00000505780.1:p.Ala88=
ENST00000370131.3:c.807A>T	ENSP00000359150.3:p.Ala269=
ENST00000370132.8:c.807A>T MANE Select	ENSP00000359151.3:p.Ala269=
NM_001918.3:c.807A>T	NP_001909.3:p.Ala269=
XM_005270545.2:c.264A>T	XP_005270602.1:p.Ala88=
XM_005270546.2:c.264A>T	XP_005270603.1:p.Ala88=
XR_946560.1:n.827A>T
XM_005270545.4:c.264A>T	XP_005270602.1:p.Ala88=
XM_017000468.2:c.264A>T	XP_016855957.1:p.Ala88=
XM_017000469.2:c.264A>T	XP_016855958.1:p.Ala88=
XR_946560.3:n.824A>T
NM_001918.4:c.807A>T	NP_001909.3:p.Ala269=
NM_001918.5:c.807A>T MANE Select	NP_001909.4:p.Ala269=
NM_001399969.1:c.264A>T	NP_001386898.1:p.Ala88=
NM_001399972.1:c.264A>T	NP_001386901.1:p.Ala88=
NR_174363.1:n.639A>T
NR_174364.1:n.821A>T
NR_174365.1:n.604A>T
NR_174366.1:n.821A>T