Canonical Allele Identifier: CA419099355

Gene: DBT

Linked Data

• MyVariant Identifiers: chr1:g.100671789A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100206233A>T , CM000663.2:g.100206233A>T	GRCh38
NC_000001.10:g.100671789A>T , CM000663.1:g.100671789A>T	GRCh37
NC_000001.9:g.100444377A>T	NCBI36
NG_011852.2:g.48621T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681617.1:c.1404T>A	ENSP00000505544.1:p.Ile468=
ENST00000681780.1:c.735T>A	ENSP00000505780.1:p.Ile245=
ENST00000370132.8:c.1278T>A MANE Select	ENSP00000359151.3:p.Ile426=
NM_001918.3:c.1278T>A	NP_001909.3:p.Ile426=
XM_005270545.2:c.735T>A	XP_005270602.1:p.Ile245=
XM_005270546.2:c.735T>A	XP_005270603.1:p.Ile245=
XM_005270545.4:c.735T>A	XP_005270602.1:p.Ile245=
XM_017000468.2:c.735T>A	XP_016855957.1:p.Ile245=
XM_017000469.2:c.735T>A	XP_016855958.1:p.Ile245=
NM_001918.4:c.1278T>A	NP_001909.3:p.Ile426=
NM_001918.5:c.1278T>A MANE Select	NP_001909.4:p.Ile426=
NM_001399969.1:c.735T>A	NP_001386898.1:p.Ile245=
NM_001399972.1:c.735T>A	NP_001386901.1:p.Ile245=
NR_174363.1:n.1110T>A
NR_174364.1:n.1292T>A
NR_174365.1:n.1075T>A
NR_174366.1:n.1377T>A