Canonical Allele Identifier: CA341345493

Gene: DBT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100235481A>G , CM000663.2:g.100235481A>G	GRCh38
NC_000001.10:g.100701037A>G , CM000663.1:g.100701037A>G	GRCh37
NC_000001.9:g.100473625A>G	NCBI36
NG_011852.2:g.19373T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001918.5:c.206T>C MANE Select	NP_001909.4:p.Leu69Pro
ENST00000370132.8:c.206T>C MANE Select	ENSP00000359151.3:p.Leu69Pro
NM_001399969.1:c.-338T>C	NP_001386898.1:n.-338T>C
NM_001399972.1:c.-338T>C	NP_001386901.1:n.-338T>C
NM_001918.3:c.206T>C	NP_001909.3:p.Leu69Pro
NM_001918.4:c.206T>C	NP_001909.3:p.Leu69Pro
NR_174363.1:n.220T>C
NR_174364.1:n.220T>C
NR_174365.1:n.220T>C
NR_174366.1:n.220T>C
ENST00000370131.3:c.206T>C	ENSP00000359150.3:p.Leu69Pro
ENST00000681617.1:c.206T>C	ENSP00000505544.1:p.Leu69Pro
ENST00000681780.1:c.-338T>C	ENSP00000505780.1:n.-338T>C
XM_005270545.2:c.-338T>C	XP_005270602.1:n.-338T>C
XM_005270545.4:c.-338T>C	XP_005270602.1:n.-338T>C
XM_005270546.2:c.-156T>C	XP_005270603.1:n.-156T>C
XM_017000468.2:c.-338T>C	XP_016855957.1:n.-338T>C
XM_017000469.2:c.-156T>C	XP_016855958.1:n.-156T>C
XR_946560.1:n.226T>C
XR_946560.3:n.223T>C