Canonical Allele Identifier: CA942371436

Gene: DRD2

Linked Data

• dbSNP Id: rs1951063025
• gnomAD v3: 11-113439017-AAGTAAAATGATAT-A
• gnomAD v4: 11-113439017-AAGTAAAATGATAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113439019_113439031del , CM000673.2:g.113439019_113439031del	GRCh38
NC_000011.9:g.113309741_113309753del , CM000673.1:g.113309741_113309753del	GRCh37
NC_000011.8:g.112814951_112814963del	NCBI36
NG_008841.1:g.41250_41262del

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.-31-14348_-31-14336del MANE Select	ENSP00000354859.3:n.-31-14348_-31-14336de...
ENST00000346454.7:c.-31-14348_-31-14336del	ENSP00000278597.5:n.-31-14348_-31-14336de...
ENST00000362072.7:c.-31-14348_-31-14336del	ENSP00000354859.3:n.-31-14348_-31-14336de...
ENST00000540600.5:n.35-14348_35-14336del
ENST00000542616.1:c.-31-14348_-31-14336del	ENSP00000441474.1:n.-31-14348_-31-14336de...
ENST00000543292.1:c.-32+8541_-32+8553del	ENSP00000438419.1:n.-32+8541_-32+8553del
NM_000795.3:c.-31-14348_-31-14336del	NP_000786.1:n.-31-14348_-31-14336del
NM_016574.3:c.-31-14348_-31-14336del	NP_057658.2:n.-31-14348_-31-14336del
XM_017017296.2:c.-31-14348_-31-14336del	XP_016872785.1:n.-31-14348_-31-14336del
NM_000795.4:c.-31-14348_-31-14336del MANE Select	NP_000786.1:n.-31-14348_-31-14336del
NM_016574.4:c.-31-14348_-31-14336del	NP_057658.2:n.-31-14348_-31-14336del