Canonical Allele Identifier: CA2001159579

Gene: DRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113439249_113439250delinsAG , CM000673.2:g.113439249_113439250delinsAG	GRCh38
NC_000011.9:g.113309971_113309972delinsAG , CM000673.1:g.113309971_113309972delinsAG	GRCh37
NC_000011.8:g.112815181_112815182delinsAG	NCBI36
NG_008841.1:g.41030_41031delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.-31-14568_-31-14567delinsCT MANE Select	ENSP00000354859.3:n.-31-14568_-31-14567de...
ENST00000346454.7:c.-31-14568_-31-14567delinsCT	ENSP00000278597.5:n.-31-14568_-31-14567de...
ENST00000362072.7:c.-31-14568_-31-14567delinsCT	ENSP00000354859.3:n.-31-14568_-31-14567de...
ENST00000540600.5:n.35-14568_35-14567delinsCT
ENST00000542616.1:c.-31-14568_-31-14567delinsCT	ENSP00000441474.1:n.-31-14568_-31-14567de...
ENST00000543292.1:c.-32+8321_-32+8322delinsCT	ENSP00000438419.1:n.-32+8321_-32+8322deli...
NM_000795.3:c.-31-14568_-31-14567delinsCT	NP_000786.1:n.-31-14568_-31-14567delinsCT...
NM_016574.3:c.-31-14568_-31-14567delinsCT	NP_057658.2:n.-31-14568_-31-14567delinsCT...
XM_017017296.2:c.-31-14568_-31-14567delinsCT	XP_016872785.1:n.-31-14568_-31-14567delin...
NM_000795.4:c.-31-14568_-31-14567delinsCT MANE Select	NP_000786.1:n.-31-14568_-31-14567delinsCT...
NM_016574.4:c.-31-14568_-31-14567delinsCT	NP_057658.2:n.-31-14568_-31-14567delinsCT...