Canonical Allele Identifier: CA969456

Gene: DBT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100196304C>T , CM000663.2:g.100196304C>T	GRCh38
NC_000001.10:g.100661860C>T , CM000663.1:g.100661860C>T	GRCh37
NC_000001.9:g.100434448C>T	NCBI36
NG_011852.2:g.58550G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001918.5:c.1400G>A MANE Select	NP_001909.4:p.Trp467Ter
ENST00000370132.8:c.1400G>A MANE Select	ENSP00000359151.3:p.Trp467Ter
NM_001399969.1:c.857G>A	NP_001386898.1:p.Trp286Ter
NM_001399972.1:c.857G>A	NP_001386901.1:p.Trp286Ter
NM_001918.3:c.1400G>A	NP_001909.3:p.Trp467Ter
NM_001918.4:c.1400G>A	NP_001909.3:p.Trp467Ter
NR_174363.1:n.1232G>A
NR_174364.1:n.1573G>A
NR_174365.1:n.1197G>A
NR_174366.1:n.1499G>A
ENST00000681617.1:c.1526G>A	ENSP00000505544.1:p.Trp509Ter
ENST00000681780.1:c.857G>A	ENSP00000505780.1:p.Trp286Ter
XM_005270545.2:c.857G>A	XP_005270602.1:p.Trp286Ter
XM_005270545.4:c.857G>A	XP_005270602.1:p.Trp286Ter
XM_005270546.2:c.857G>A	XP_005270603.1:p.Trp286Ter
XM_017000468.2:c.857G>A	XP_016855957.1:p.Trp286Ter
XM_017000469.2:c.857G>A	XP_016855958.1:p.Trp286Ter