Canonical Allele Identifier: CA2001161849

Gene: DRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113442641_113442642delinsTG , CM000673.2:g.113442641_113442642delinsTG	GRCh38
NC_000011.9:g.113313363_113313364delinsTG , CM000673.1:g.113313363_113313364delinsTG	GRCh37
NC_000011.8:g.112818573_112818574delinsTG	NCBI36
NG_008841.1:g.37638_37639delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.-31-17960_-31-17959delinsCA MANE Select	ENSP00000354859.3:n.-31-17960_-31-17959de...
ENST00000346454.7:c.-31-17960_-31-17959delinsCA	ENSP00000278597.5:n.-31-17960_-31-17959de...
ENST00000362072.7:c.-31-17960_-31-17959delinsCA	ENSP00000354859.3:n.-31-17960_-31-17959de...
ENST00000540600.5:n.35-17960_35-17959delinsCA
ENST00000542616.1:c.-31-17960_-31-17959delinsCA	ENSP00000441474.1:n.-31-17960_-31-17959de...
ENST00000543292.1:c.-32+4929_-32+4930delinsCA	ENSP00000438419.1:n.-32+4929_-32+4930deli...
NM_000795.3:c.-31-17960_-31-17959delinsCA	NP_000786.1:n.-31-17960_-31-17959delinsCA...
NM_016574.3:c.-31-17960_-31-17959delinsCA	NP_057658.2:n.-31-17960_-31-17959delinsCA...
XM_017017296.2:c.-31-17960_-31-17959delinsCA	XP_016872785.1:n.-31-17960_-31-17959delin...
NM_000795.4:c.-31-17960_-31-17959delinsCA MANE Select	NP_000786.1:n.-31-17960_-31-17959delinsCA...
NM_016574.4:c.-31-17960_-31-17959delinsCA	NP_057658.2:n.-31-17960_-31-17959delinsCA...