Canonical Allele Identifier: CA1184062341

Gene: DBT

Linked Data

• dbSNP Id: rs1662405062

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100215132_100215136del , CM000663.2:g.100215132_100215136del	GRCh38
NC_000001.10:g.100680688_100680692del , CM000663.1:g.100680688_100680692del	GRCh37
NC_000001.9:g.100453276_100453280del	NCBI36
NG_011852.2:g.39725_39729del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681617.1:c.773-146_773-142del	ENSP00000505544.1:n.773-146_773-142del
ENST00000681780.1:c.230-146_230-142del	ENSP00000505780.1:n.230-146_230-142del
ENST00000370131.3:c.773-146_773-142del	ENSP00000359150.3:n.773-146_773-142del
ENST00000370132.8:c.773-146_773-142del MANE Select	ENSP00000359151.3:n.773-146_773-142del
NM_001918.3:c.773-146_773-142del	NP_001909.3:n.773-146_773-142del
XM_005270545.2:c.230-146_230-142del	XP_005270602.1:n.230-146_230-142del
XM_005270546.2:c.230-146_230-142del	XP_005270603.1:n.230-146_230-142del
XR_946560.1:n.793-146_793-142del
XM_005270545.4:c.230-146_230-142del	XP_005270602.1:n.230-146_230-142del
XM_017000468.2:c.230-146_230-142del	XP_016855957.1:n.230-146_230-142del
XM_017000469.2:c.230-146_230-142del	XP_016855958.1:n.230-146_230-142del
XR_946560.3:n.790-146_790-142del
NM_001918.4:c.773-146_773-142del	NP_001909.3:n.773-146_773-142del
NM_001918.5:c.773-146_773-142del MANE Select	NP_001909.4:n.773-146_773-142del
NM_001399969.1:c.230-146_230-142del	NP_001386898.1:n.230-146_230-142del
NM_001399972.1:c.230-146_230-142del	NP_001386901.1:n.230-146_230-142del
NR_174363.1:n.605-146_605-142del
NR_174364.1:n.787-146_787-142del
NR_174365.1:n.570-146_570-142del
NR_174366.1:n.787-146_787-142del