Canonical Allele Identifier: CA969567

Gene: DBT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100206522G>A , CM000663.2:g.100206522G>A	GRCh38
NC_000001.10:g.100672078G>A , CM000663.1:g.100672078G>A	GRCh37
NC_000001.9:g.100444666G>A	NCBI36
NG_011852.2:g.48332C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001918.5:c.1132C>T MANE Select	NP_001909.4:p.Gln378Ter
ENST00000370132.8:c.1132C>T MANE Select	ENSP00000359151.3:p.Gln378Ter
NM_001399969.1:c.589C>T	NP_001386898.1:p.Gln197Ter
NM_001399972.1:c.589C>T	NP_001386901.1:p.Gln197Ter
NM_001918.3:c.1132C>T	NP_001909.3:p.Gln378Ter
NM_001918.4:c.1132C>T	NP_001909.3:p.Gln378Ter
NR_174363.1:n.964C>T
NR_174364.1:n.1146C>T
NR_174365.1:n.929C>T
NR_174366.1:n.1231C>T
ENST00000681617.1:c.1258C>T	ENSP00000505544.1:p.Gln420Ter
ENST00000681780.1:c.589C>T	ENSP00000505780.1:p.Gln197Ter
XM_005270545.2:c.589C>T	XP_005270602.1:p.Gln197Ter
XM_005270545.4:c.589C>T	XP_005270602.1:p.Gln197Ter
XM_005270546.2:c.589C>T	XP_005270603.1:p.Gln197Ter
XM_017000468.2:c.589C>T	XP_016855957.1:p.Gln197Ter
XM_017000469.2:c.589C>T	XP_016855958.1:p.Gln197Ter