Canonical Allele Identifier: CA341343394

Gene: DBT

Linked Data

• MyVariant Identifiers: chr1:g.100696301C>G (hg19) ; chr1:g.100230745C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100230745C>G , CM000663.2:g.100230745C>G	GRCh38
NC_000001.10:g.100696301C>G , CM000663.1:g.100696301C>G	GRCh37
NC_000001.9:g.100468889C>G	NCBI36
NG_011852.2:g.24109G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681617.1:c.421G>C	ENSP00000505544.1:p.Glu141Gln
ENST00000681780.1:c.-123G>C	ENSP00000505780.1:n.-123G>C
ENST00000370131.3:c.421G>C	ENSP00000359150.3:p.Glu141Gln
ENST00000370132.8:c.421G>C MANE Select	ENSP00000359151.3:p.Glu141Gln
NM_001918.3:c.421G>C	NP_001909.3:p.Glu141Gln
XM_005270545.2:c.-123G>C	XP_005270602.1:n.-123G>C
XM_005270546.2:c.-111+4691G>C	XP_005270603.1:n.-111+4691G>C
XR_946560.1:n.441G>C
XM_005270545.4:c.-123G>C	XP_005270602.1:n.-123G>C
XM_017000468.2:c.-123G>C	XP_016855957.1:n.-123G>C
XM_017000469.2:c.-111+4691G>C	XP_016855958.1:n.-111+4691G>C
XR_946560.3:n.438G>C
NM_001918.4:c.421G>C	NP_001909.3:p.Glu141Gln
NM_001918.5:c.421G>C MANE Select	NP_001909.4:p.Glu141Gln
NM_001399969.1:c.-123G>C	NP_001386898.1:n.-123G>C
NM_001399972.1:c.-123G>C	NP_001386901.1:n.-123G>C
NR_174363.1:n.265+4691G>C
NR_174364.1:n.435G>C
NR_174365.1:n.435G>C
NR_174366.1:n.435G>C