Canonical Allele Identifier: CA1184062284

Gene: DBT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100214977T= , CM000663.2:g.100214977T=	GRCh38
NC_000001.10:g.100680533T= , CM000663.1:g.100680533T=	GRCh37
NC_000001.9:g.100453121T=	NCBI36
NG_011852.2:g.39877A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681617.1:c.779A=	ENSP00000505544.1:p.Gln260=
ENST00000681780.1:c.236A=	ENSP00000505780.1:p.Gln79=
ENST00000370131.3:c.779A=	ENSP00000359150.3:p.Gln260=
ENST00000370132.8:c.779A= MANE Select	ENSP00000359151.3:p.Gln260=
NM_001918.3:c.779A=	NP_001909.3:p.Gln260=
XM_005270545.2:c.236A=	XP_005270602.1:p.Gln79=
XM_005270546.2:c.236A=	XP_005270603.1:p.Gln79=
XR_946560.1:n.799A=
XM_005270545.4:c.236A=	XP_005270602.1:p.Gln79=
XM_017000468.2:c.236A=	XP_016855957.1:p.Gln79=
XM_017000469.2:c.236A=	XP_016855958.1:p.Gln79=
XR_946560.3:n.796A=
NM_001918.4:c.779A=	NP_001909.3:p.Gln260=
NM_001918.5:c.779A= MANE Select	NP_001909.4:p.Gln260=
NM_001399969.1:c.236A=	NP_001386898.1:p.Gln79=
NM_001399972.1:c.236A=	NP_001386901.1:p.Gln79=
NR_174363.1:n.611A=
NR_174364.1:n.793A=
NR_174365.1:n.576A=
NR_174366.1:n.793A=