Canonical Allele Identifier: CA419101360

Gene: DBT

Linked Data

• MyVariant Identifiers: chr1:g.100680448A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100214892A>G , CM000663.2:g.100214892A>G	GRCh38
NC_000001.10:g.100680448A>G , CM000663.1:g.100680448A>G	GRCh37
NC_000001.9:g.100453036A>G	NCBI36
NG_011852.2:g.39962T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681617.1:c.864T>C	ENSP00000505544.1:p.Val288=
ENST00000681780.1:c.321T>C	ENSP00000505780.1:p.Val107=
ENST00000370131.3:c.864T>C	ENSP00000359150.3:p.Val288=
ENST00000370132.8:c.864T>C MANE Select	ENSP00000359151.3:p.Val288=
NM_001918.3:c.864T>C	NP_001909.3:p.Val288=
XM_005270545.2:c.321T>C	XP_005270602.1:p.Val107=
XM_005270546.2:c.321T>C	XP_005270603.1:p.Val107=
XR_946560.1:n.884T>C
XM_005270545.4:c.321T>C	XP_005270602.1:p.Val107=
XM_017000468.2:c.321T>C	XP_016855957.1:p.Val107=
XM_017000469.2:c.321T>C	XP_016855958.1:p.Val107=
XR_946560.3:n.881T>C
NM_001918.4:c.864T>C	NP_001909.3:p.Val288=
NM_001918.5:c.864T>C MANE Select	NP_001909.4:p.Val288=
NM_001399969.1:c.321T>C	NP_001386898.1:p.Val107=
NM_001399972.1:c.321T>C	NP_001386901.1:p.Val107=
NR_174363.1:n.696T>C
NR_174364.1:n.878T>C
NR_174365.1:n.661T>C
NR_174366.1:n.878T>C