Canonical Allele Identifier: CA1184058936

Gene: DBT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100206420T= , CM000663.2:g.100206420T=	GRCh38
NC_000001.10:g.100671976T= , CM000663.1:g.100671976T=	GRCh37
NC_000001.9:g.100444564T=	NCBI36
NG_011852.2:g.48434A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000681617.1:c.1335+25A=	ENSP00000505544.1:n.1335+25A=
ENST00000681780.1:c.666+25A=	ENSP00000505780.1:n.666+25A=
ENST00000370132.8:c.1209+25A= MANE Select	ENSP00000359151.3:n.1209+25A=
NM_001918.3:c.1209+25A=	NP_001909.3:n.1209+25A=
XM_005270545.2:c.666+25A=	XP_005270602.1:n.666+25A=
XM_005270546.2:c.666+25A=	XP_005270603.1:n.666+25A=
XM_005270545.4:c.666+25A=	XP_005270602.1:n.666+25A=
XM_017000468.2:c.666+25A=	XP_016855957.1:n.666+25A=
XM_017000469.2:c.666+25A=	XP_016855958.1:n.666+25A=
NM_001918.4:c.1209+25A=	NP_001909.3:n.1209+25A=
NM_001918.5:c.1209+25A= MANE Select	NP_001909.4:n.1209+25A=
NM_001399969.1:c.666+25A=	NP_001386898.1:n.666+25A=
NM_001399972.1:c.666+25A=	NP_001386901.1:n.666+25A=
NR_174363.1:n.1041+25A=
NR_174364.1:n.1223+25A=
NR_174365.1:n.1006+25A=
NR_174366.1:n.1308+25A=