Canonical Allele Identifier: CA10016742

Gene: DOP1B

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.36239795C>T , CM000683.2:g.36239795C>T	GRCh38
NC_000021.8:g.37612093C>T , CM000683.1:g.37612093C>T	GRCh37
NC_000021.7:g.36533963C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001320714.2:c.2907C>T MANE Select	NP_001307643.1:p.Ala969=
ENST00000691173.1:c.2907C>T MANE Select	ENSP00000509598.1:p.Ala969=
NM_001320714.1:c.2907C>T	NP_001307643.1:p.Ala969=
NM_005128.3:c.2907C>T	NP_005119.2:p.Ala969=
NM_005128.4:c.2907C>T	NP_005119.2:p.Ala969=
ENST00000399151.3:c.2907C>T	ENSP00000382104.3:p.Ala969=
ENST00000685394.1:c.2907C>T	ENSP00000510500.1:p.Ala969=
ENST00000693273.1:c.*1882C>T	ENSP00000510799.1:n.*1882C>T
XM_006724068.1:c.2907C>T	XP_006724131.1:p.Ala969=
XM_017028509.1:c.2253C>T	XP_016883998.1:p.Ala751=
XR_001754923.2:n.3096C>T
XR_937581.1:n.3092C>T
XR_937581.3:n.3095C>T
XR_937582.1:n.3094C>T