Canonical Allele Identifier: CA382649898

Gene: DRD2

Linked Data

• MyVariant Identifiers: chr11:g.113283391T>A (hg19) ; chr11:g.113412669T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113412669T>A , CM000673.2:g.113412669T>A	GRCh38
NC_000011.9:g.113283391T>A , CM000673.1:g.113283391T>A	GRCh37
NC_000011.8:g.112788601T>A	NCBI36
NG_008841.1:g.67611A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.1025A>T MANE Select	ENSP00000354859.3:p.Glu342Val
ENST00000346454.7:c.938A>T	ENSP00000278597.5:p.Glu313Val
ENST00000362072.7:c.1025A>T	ENSP00000354859.3:p.Glu342Val
ENST00000538967.5:c.1031A>T	ENSP00000438215.1:p.Glu344Val
ENST00000542968.5:c.1025A>T	ENSP00000442172.1:p.Glu342Val
ENST00000544518.5:c.1022A>T	ENSP00000441068.1:p.Glu341Val
NM_000795.3:c.1025A>T	NP_000786.1:p.Glu342Val
NM_016574.3:c.938A>T	NP_057658.2:p.Glu313Val
XM_017017296.2:c.1025A>T	XP_016872785.1:p.Glu342Val
NM_000795.4:c.1025A>T MANE Select	NP_000786.1:p.Glu342Val
NM_016574.4:c.938A>T	NP_057658.2:p.Glu313Val