Canonical Allele Identifier: CA382648968

Gene: DRD2

Linked Data

• gnomAD v4: 11-113410752-G-A
• MyVariant Identifiers: chr11:g.113281474G>A (hg19) ; chr11:g.113410752G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113410752G>A , CM000673.2:g.113410752G>A	GRCh38
NC_000011.9:g.113281474G>A , CM000673.1:g.113281474G>A	GRCh37
NC_000011.8:g.112786684G>A	NCBI36
NG_008841.1:g.69528C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.1307C>T MANE Select	ENSP00000354859.3:p.Ala436Val
ENST00000346454.7:c.1220C>T	ENSP00000278597.5:p.Ala407Val
ENST00000362072.7:c.1307C>T	ENSP00000354859.3:p.Ala436Val
ENST00000538967.5:c.1313C>T	ENSP00000438215.1:p.Ala438Val
ENST00000542968.5:c.1307C>T	ENSP00000442172.1:p.Ala436Val
ENST00000544518.5:c.1304C>T	ENSP00000441068.1:p.Ala435Val
NM_000795.3:c.1307C>T	NP_000786.1:p.Ala436Val
NM_016574.3:c.1220C>T	NP_057658.2:p.Ala407Val
XM_017017296.2:c.1307C>T	XP_016872785.1:p.Ala436Val
NM_000795.4:c.1307C>T MANE Select	NP_000786.1:p.Ala436Val
NM_016574.4:c.1220C>T	NP_057658.2:p.Ala407Val