Canonical Allele Identifier: CA341332590

Gene: DBT

Linked Data

• MyVariant Identifiers: chr1:g.100672177C>G (hg19) ; chr1:g.100206621C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100206621C>G , CM000663.2:g.100206621C>G	GRCh38
NC_000001.10:g.100672177C>G , CM000663.1:g.100672177C>G	GRCh37
NC_000001.9:g.100444765C>G	NCBI36
NG_011852.2:g.48233G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681617.1:c.1159G>C	ENSP00000505544.1:p.Gly387Arg
ENST00000681780.1:c.490G>C	ENSP00000505780.1:p.Gly164Arg
ENST00000370132.8:c.1033G>C MANE Select	ENSP00000359151.3:p.Gly345Arg
NM_001918.3:c.1033G>C	NP_001909.3:p.Gly345Arg
XM_005270545.2:c.490G>C	XP_005270602.1:p.Gly164Arg
XM_005270546.2:c.490G>C	XP_005270603.1:p.Gly164Arg
XM_005270545.4:c.490G>C	XP_005270602.1:p.Gly164Arg
XM_017000468.2:c.490G>C	XP_016855957.1:p.Gly164Arg
XM_017000469.2:c.490G>C	XP_016855958.1:p.Gly164Arg
NM_001918.4:c.1033G>C	NP_001909.3:p.Gly345Arg
NM_001918.5:c.1033G>C MANE Select	NP_001909.4:p.Gly345Arg
NM_001399969.1:c.490G>C	NP_001386898.1:p.Gly164Arg
NM_001399972.1:c.490G>C	NP_001386901.1:p.Gly164Arg
NR_174363.1:n.865G>C
NR_174364.1:n.1047G>C
NR_174365.1:n.830G>C
NR_174366.1:n.1132G>C