Canonical Allele Identifier: CA10016341

Gene: DOP1B

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.36227709C>T , CM000683.2:g.36227709C>T	GRCh38
NC_000021.8:g.37600007C>T , CM000683.1:g.37600007C>T	GRCh37
NC_000021.7:g.36521877C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001320714.2:c.1497C>T MANE Select	NP_001307643.1:p.Thr499=
ENST00000691173.1:c.1497C>T MANE Select	ENSP00000509598.1:p.Thr499=
NM_001320714.1:c.1497C>T	NP_001307643.1:p.Thr499=
NM_005128.3:c.1497C>T	NP_005119.2:p.Thr499=
NM_005128.4:c.1497C>T	NP_005119.2:p.Thr499=
ENST00000399151.3:c.1497C>T	ENSP00000382104.3:p.Thr499=
ENST00000685394.1:c.1497C>T	ENSP00000510500.1:p.Thr499=
ENST00000693273.1:c.*472C>T	ENSP00000510799.1:n.*472C>T
XM_006724068.1:c.1497C>T	XP_006724131.1:p.Thr499=
XM_017028509.1:c.843C>T	XP_016883998.1:p.Thr281=
XR_001754923.2:n.1686C>T
XR_937581.1:n.1682C>T
XR_937581.3:n.1685C>T
XR_937582.1:n.1684C>T