Canonical Allele Identifier: CA382650345

Gene: DRD2

Linked Data

• MyVariant Identifiers: chr11:g.113283502A>G (hg19) ; chr11:g.113412780A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113412780A>G , CM000673.2:g.113412780A>G	GRCh38
NC_000011.9:g.113283502A>G , CM000673.1:g.113283502A>G	GRCh37
NC_000011.8:g.112788712A>G	NCBI36
NG_008841.1:g.67500T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.914T>C MANE Select	ENSP00000354859.3:p.Leu305Pro
ENST00000346454.7:c.827T>C	ENSP00000278597.5:p.Leu276Pro
ENST00000362072.7:c.914T>C	ENSP00000354859.3:p.Leu305Pro
ENST00000538967.5:c.920T>C	ENSP00000438215.1:p.Leu307Pro
ENST00000542968.5:c.914T>C	ENSP00000442172.1:p.Leu305Pro
ENST00000544518.5:c.911T>C	ENSP00000441068.1:p.Leu304Pro
NM_000795.3:c.914T>C	NP_000786.1:p.Leu305Pro
NM_016574.3:c.827T>C	NP_057658.2:p.Leu276Pro
XM_017017296.2:c.914T>C	XP_016872785.1:p.Leu305Pro
NM_000795.4:c.914T>C MANE Select	NP_000786.1:p.Leu305Pro
NM_016574.4:c.827T>C	NP_057658.2:p.Leu276Pro