Canonical Allele Identifier: CA341334968

Gene: DBT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100210745A>C , CM000663.2:g.100210745A>C	GRCh38
NC_000001.10:g.100676301A>C , CM000663.1:g.100676301A>C	GRCh37
NC_000001.9:g.100448889A>C	NCBI36
NG_011852.2:g.44109T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001918.5:c.966T>G MANE Select	NP_001909.4:p.Phe322Leu
ENST00000370132.8:c.966T>G MANE Select	ENSP00000359151.3:p.Phe322Leu
NM_001399969.1:c.423T>G	NP_001386898.1:p.Phe141Leu
NM_001399972.1:c.423T>G	NP_001386901.1:p.Phe141Leu
NM_001918.3:c.966T>G	NP_001909.3:p.Phe322Leu
NM_001918.4:c.966T>G	NP_001909.3:p.Phe322Leu
NR_174363.1:n.798T>G
NR_174364.1:n.980T>G
NR_174365.1:n.763T>G
NR_174366.1:n.1065T>G
ENST00000370131.3:c.1319T>G	ENSP00000359150.3:n.1319T>G
ENST00000681617.1:c.1092T>G	ENSP00000505544.1:p.Phe364Leu
ENST00000681780.1:c.423T>G	ENSP00000505780.1:p.Phe141Leu
XM_005270545.2:c.423T>G	XP_005270602.1:p.Phe141Leu
XM_005270545.4:c.423T>G	XP_005270602.1:p.Phe141Leu
XM_005270546.2:c.423T>G	XP_005270603.1:p.Phe141Leu
XM_017000468.2:c.423T>G	XP_016855957.1:p.Phe141Leu
XM_017000469.2:c.423T>G	XP_016855958.1:p.Phe141Leu
XR_946560.1:n.1071T>G
XR_946560.3:n.1068T>G