Canonical Allele Identifier: CA210950

Gene: DBT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100206504T= , CM000663.2:g.100206504T=	GRCh38
NC_000001.10:g.100672060T= , CM000663.1:g.100672060T=	GRCh37
NC_000001.9:g.100444648T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001918.5:c.1150A= MANE Select	NP_001909.4:p.Ser384=
ENST00000370132.8:c.1150A= MANE Select	ENSP00000359151.3:p.Ser384=
NM_001399969.1:c.607A=	NP_001386898.1:p.Ser203=
NM_001399972.1:c.607A=	NP_001386901.1:p.Ser203=
NR_174363.1:n.982A=
NR_174364.1:n.1164A=
NR_174365.1:n.947A=
NR_174366.1:n.1249A=
ENST00000681617.1:c.1276A=	ENSP00000505544.1:p.Ser426=
ENST00000681780.1:c.607A=	ENSP00000505780.1:p.Ser203=
XM_005270545.2:c.607A=	XP_005270602.1:p.Ser203=
XM_005270545.4:c.607A=	XP_005270602.1:p.Ser203=
XM_005270546.2:c.607A=	XP_005270603.1:p.Ser203=
XM_017000468.2:c.607A=	XP_016855957.1:p.Ser203=
XM_017000469.2:c.607A=	XP_016855958.1:p.Ser203=