Canonical Allele Identifier: CA2001159603

Gene: DRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113439288_113439289delinsGT , CM000673.2:g.113439288_113439289delinsGT	GRCh38
NC_000011.9:g.113310010_113310011delinsGT , CM000673.1:g.113310010_113310011delinsGT	GRCh37
NC_000011.8:g.112815220_112815221delinsGT	NCBI36
NG_008841.1:g.40991_40992delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.-31-14607_-31-14606delinsAC MANE Select	ENSP00000354859.3:n.-31-14607_-31-14606delinsAC
ENST00000346454.7:c.-31-14607_-31-14606delinsAC	ENSP00000278597.5:n.-31-14607_-31-14606delinsAC
ENST00000362072.7:c.-31-14607_-31-14606delinsAC	ENSP00000354859.3:n.-31-14607_-31-14606delinsAC
ENST00000540600.5:n.35-14607_35-14606delinsAC
ENST00000542616.1:c.-31-14607_-31-14606delinsAC	ENSP00000441474.1:n.-31-14607_-31-14606delinsAC
ENST00000543292.1:c.-32+8282_-32+8283delinsAC	ENSP00000438419.1:n.-32+8282_-32+8283delinsAC
NM_000795.3:c.-31-14607_-31-14606delinsAC	NP_000786.1:n.-31-14607_-31-14606delinsAC
NM_016574.3:c.-31-14607_-31-14606delinsAC	NP_057658.2:n.-31-14607_-31-14606delinsAC
XM_017017296.2:c.-31-14607_-31-14606delinsAC	XP_016872785.1:n.-31-14607_-31-14606delinsAC
NM_000795.4:c.-31-14607_-31-14606delinsAC MANE Select	NP_000786.1:n.-31-14607_-31-14606delinsAC
NM_016574.4:c.-31-14607_-31-14606delinsAC	NP_057658.2:n.-31-14607_-31-14606delinsAC