Canonical Allele Identifier: CA1184058800

Gene: DBT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100206130A= , CM000663.2:g.100206130A=	GRCh38
NC_000001.10:g.100671686A= , CM000663.1:g.100671686A=	GRCh37
NC_000001.9:g.100444274A=	NCBI36
NG_011852.2:g.48724T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681617.1:c.1407+100T=	ENSP00000505544.1:n.1407+100T=
ENST00000681780.1:c.738+100T=	ENSP00000505780.1:n.738+100T=
ENST00000370132.8:c.1281+100T= MANE Select	ENSP00000359151.3:n.1281+100T=
NM_001918.3:c.1281+100T=	NP_001909.3:n.1281+100T=
XM_005270545.2:c.738+100T=	XP_005270602.1:n.738+100T=
XM_005270546.2:c.738+100T=	XP_005270603.1:n.738+100T=
XM_005270545.4:c.738+100T=	XP_005270602.1:n.738+100T=
XM_017000468.2:c.738+100T=	XP_016855957.1:n.738+100T=
XM_017000469.2:c.738+100T=	XP_016855958.1:n.738+100T=
NM_001918.4:c.1281+100T=	NP_001909.3:n.1281+100T=
NM_001918.5:c.1281+100T= MANE Select	NP_001909.4:n.1281+100T=
NM_001399969.1:c.738+100T=	NP_001386898.1:n.738+100T=
NM_001399972.1:c.738+100T=	NP_001386901.1:n.738+100T=
NR_174363.1:n.1113+100T=
NR_174364.1:n.1295+100T=
NR_174365.1:n.1078+100T=
NR_174366.1:n.1380+100T=