Canonical Allele Identifier: CA382649050

Gene: DRD2

Linked Data

• MyVariant Identifiers: chr11:g.113281508T>A (hg19) ; chr11:g.113410786T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113410786T>A , CM000673.2:g.113410786T>A	GRCh38
NC_000011.9:g.113281508T>A , CM000673.1:g.113281508T>A	GRCh37
NC_000011.8:g.112786718T>A	NCBI36
NG_008841.1:g.69494A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.1273A>T MANE Select	ENSP00000354859.3:p.Ile425Phe
ENST00000346454.7:c.1186A>T	ENSP00000278597.5:p.Ile396Phe
ENST00000362072.7:c.1273A>T	ENSP00000354859.3:p.Ile425Phe
ENST00000538967.5:c.1279A>T	ENSP00000438215.1:p.Ile427Phe
ENST00000542968.5:c.1273A>T	ENSP00000442172.1:p.Ile425Phe
ENST00000544518.5:c.1270A>T	ENSP00000441068.1:p.Ile424Phe
NM_000795.3:c.1273A>T	NP_000786.1:p.Ile425Phe
NM_016574.3:c.1186A>T	NP_057658.2:p.Ile396Phe
XM_017017296.2:c.1273A>T	XP_016872785.1:p.Ile425Phe
NM_000795.4:c.1273A>T MANE Select	NP_000786.1:p.Ile425Phe
NM_016574.4:c.1186A>T	NP_057658.2:p.Ile396Phe