Canonical Allele Identifier: CA2001159743

Gene: DRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113439555_113439556delinsCA , CM000673.2:g.113439555_113439556delinsCA	GRCh38
NC_000011.9:g.113310277_113310278delinsCA , CM000673.1:g.113310277_113310278delinsCA	GRCh37
NC_000011.8:g.112815487_112815488delinsCA	NCBI36
NG_008841.1:g.40724_40725delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.-31-14874_-31-14873delinsTG MANE Select	ENSP00000354859.3:n.-31-14874_-31-14873delinsTG
ENST00000346454.7:c.-31-14874_-31-14873delinsTG	ENSP00000278597.5:n.-31-14874_-31-14873delinsTG
ENST00000362072.7:c.-31-14874_-31-14873delinsTG	ENSP00000354859.3:n.-31-14874_-31-14873delinsTG
ENST00000540600.5:n.35-14874_35-14873delinsTG
ENST00000542616.1:c.-31-14874_-31-14873delinsTG	ENSP00000441474.1:n.-31-14874_-31-14873delinsTG
ENST00000543292.1:c.-32+8015_-32+8016delinsTG	ENSP00000438419.1:n.-32+8015_-32+8016delinsTG
NM_000795.3:c.-31-14874_-31-14873delinsTG	NP_000786.1:n.-31-14874_-31-14873delinsTG
NM_016574.3:c.-31-14874_-31-14873delinsTG	NP_057658.2:n.-31-14874_-31-14873delinsTG
XM_017017296.2:c.-31-14874_-31-14873delinsTG	XP_016872785.1:n.-31-14874_-31-14873delinsTG
NM_000795.4:c.-31-14874_-31-14873delinsTG MANE Select	NP_000786.1:n.-31-14874_-31-14873delinsTG
NM_016574.4:c.-31-14874_-31-14873delinsTG	NP_057658.2:n.-31-14874_-31-14873delinsTG