Canonical Allele Identifier: CA969877

Gene: DBT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100249820T>C , CM000663.2:g.100249820T>C	GRCh38
NC_000001.10:g.100715376T>C , CM000663.1:g.100715376T>C	GRCh37
NC_000001.9:g.100487964T>C	NCBI36
NG_011852.2:g.5034A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001918.5:c.1A>G MANE Select	NP_001909.4:p.Met1Val
ENST00000370132.8:c.1A>G MANE Select	ENSP00000359151.3:p.Met1Val
NM_001399969.1:c.-730A>G	NP_001386898.1:n.-730A>G
NM_001399972.1:c.-603A>G	NP_001386901.1:n.-603A>G
NM_001918.3:c.1A>G	NP_001909.3:p.Met1Val
NM_001918.4:c.1A>G	NP_001909.3:p.Met1Val
NR_174363.1:n.15A>G
NR_174364.1:n.15A>G
NR_174365.1:n.15A>G
NR_174366.1:n.15A>G
ENST00000370131.3:c.1A>G	ENSP00000359150.3:p.Met1Val
ENST00000681617.1:c.1A>G	ENSP00000505544.1:p.Met1Val
ENST00000681780.1:c.-730A>G	ENSP00000505780.1:n.-730A>G
XM_005270545.2:c.-730A>G	XP_005270602.1:n.-730A>G
XM_005270545.4:c.-730A>G	XP_005270602.1:n.-730A>G
XM_017000468.2:c.-790A>G	XP_016855957.1:n.-790A>G
XR_946560.1:n.21A>G
XR_946560.3:n.18A>G