Canonical Allele Identifier: CA27598827

Gene: DBT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100195866T>C , CM000663.2:g.100195866T>C	GRCh38
NC_000001.10:g.100661422T>C , CM000663.1:g.100661422T>C	GRCh37
NC_000001.9:g.100434010T>C	NCBI36
NG_011852.2:g.58988A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001918.5:c.*389A>G MANE Select	NP_001909.4:n.*389A>G
ENST00000370132.8:c.*389A>G MANE Select	ENSP00000359151.3:n.*389A>G
NM_001399969.1:c.*389A>G	NP_001386898.1:n.*389A>G
NM_001399972.1:c.*389A>G	NP_001386901.1:n.*389A>G
NM_001918.3:c.*389A>G	NP_001909.3:n.*389A>G
NM_001918.4:c.*389A>G	NP_001909.3:n.*389A>G
NR_174363.1:n.1670A>G
NR_174364.1:n.2011A>G
NR_174365.1:n.1635A>G
NR_174366.1:n.1937A>G
ENST00000681617.1:c.*389A>G	ENSP00000505544.1:n.*389A>G
XM_005270545.2:c.*389A>G	XP_005270602.1:n.*389A>G
XM_005270545.4:c.*389A>G	XP_005270602.1:n.*389A>G
XM_005270546.2:c.*389A>G	XP_005270603.1:n.*389A>G
XM_017000468.2:c.*389A>G	XP_016855957.1:n.*389A>G
XM_017000469.2:c.*389A>G	XP_016855958.1:n.*389A>G