Canonical Allele Identifier: CA476817032

Gene: DRD2

Linked Data

• MyVariant Identifiers: chr11:g.113281512G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113410790G>T , CM000673.2:g.113410790G>T	GRCh38
NC_000011.9:g.113281512G>T , CM000673.1:g.113281512G>T	GRCh37
NC_000011.8:g.112786722G>T	NCBI36
NG_008841.1:g.69490C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.1269C>A MANE Select	ENSP00000354859.3:p.Pro423=
ENST00000346454.7:c.1182C>A	ENSP00000278597.5:p.Pro394=
ENST00000362072.7:c.1269C>A	ENSP00000354859.3:p.Pro423=
ENST00000538967.5:c.1275C>A	ENSP00000438215.1:p.Pro425=
ENST00000542968.5:c.1269C>A	ENSP00000442172.1:p.Pro423=
ENST00000544518.5:c.1266C>A	ENSP00000441068.1:p.Pro422=
NM_000795.3:c.1269C>A	NP_000786.1:p.Pro423=
NM_016574.3:c.1182C>A	NP_057658.2:p.Pro394=
XM_017017296.2:c.1269C>A	XP_016872785.1:p.Pro423=
NM_000795.4:c.1269C>A MANE Select	NP_000786.1:p.Pro423=
NM_016574.4:c.1182C>A	NP_057658.2:p.Pro394=