Canonical Allele Identifier: CA382648946

Gene: DRD2

Linked Data

• MyVariant Identifiers: chr11:g.113281463T>G (hg19) ; chr11:g.113410741T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113410741T>G , CM000673.2:g.113410741T>G	GRCh38
NC_000011.9:g.113281463T>G , CM000673.1:g.113281463T>G	GRCh37
NC_000011.8:g.112786673T>G	NCBI36
NG_008841.1:g.69539A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.1318A>C MANE Select	ENSP00000354859.3:p.Ile440Leu
ENST00000346454.7:c.1231A>C	ENSP00000278597.5:p.Ile411Leu
ENST00000362072.7:c.1318A>C	ENSP00000354859.3:p.Ile440Leu
ENST00000538967.5:c.1324A>C	ENSP00000438215.1:p.Ile442Leu
ENST00000542968.5:c.1318A>C	ENSP00000442172.1:p.Ile440Leu
ENST00000544518.5:c.1315A>C	ENSP00000441068.1:p.Ile439Leu
NM_000795.3:c.1318A>C	NP_000786.1:p.Ile440Leu
NM_016574.3:c.1231A>C	NP_057658.2:p.Ile411Leu
XM_017017296.2:c.1318A>C	XP_016872785.1:p.Ile440Leu
NM_000795.4:c.1318A>C MANE Select	NP_000786.1:p.Ile440Leu
NM_016574.4:c.1231A>C	NP_057658.2:p.Ile411Leu