Canonical Allele Identifier: CA382649122

Gene: DRD2

Linked Data

• MyVariant Identifiers: chr11:g.113281540A>G (hg19) ; chr11:g.113410818A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113410818A>G , CM000673.2:g.113410818A>G	GRCh38
NC_000011.9:g.113281540A>G , CM000673.1:g.113281540A>G	GRCh37
NC_000011.8:g.112786750A>G	NCBI36
NG_008841.1:g.69462T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.1241T>C MANE Select	ENSP00000354859.3:p.Leu414Pro
ENST00000346454.7:c.1154T>C	ENSP00000278597.5:p.Leu385Pro
ENST00000362072.7:c.1241T>C	ENSP00000354859.3:p.Leu414Pro
ENST00000538967.5:c.1247T>C	ENSP00000438215.1:p.Leu416Pro
ENST00000542968.5:c.1241T>C	ENSP00000442172.1:p.Leu414Pro
ENST00000544518.5:c.1238T>C	ENSP00000441068.1:p.Leu413Pro
NM_000795.3:c.1241T>C	NP_000786.1:p.Leu414Pro
NM_016574.3:c.1154T>C	NP_057658.2:p.Leu385Pro
XM_017017296.2:c.1241T>C	XP_016872785.1:p.Leu414Pro
NM_000795.4:c.1241T>C MANE Select	NP_000786.1:p.Leu414Pro
NM_016574.4:c.1154T>C	NP_057658.2:p.Leu385Pro