Canonical Allele Identifier: CA15709267

Gene: DRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113418315G>A , CM000673.2:g.113418315G>A	GRCh38
NC_000011.9:g.113289037G>A , CM000673.1:g.113289037G>A	GRCh37
NC_000011.8:g.112794247G>A	NCBI36
NG_008841.1:g.61965C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000795.4:c.286-179C>T MANE Select	NP_000786.1:n.286-179C>T
ENST00000362072.8:c.286-179C>T MANE Select	ENSP00000354859.3:n.286-179C>T
NM_000795.3:c.286-179C>T	NP_000786.1:n.286-179C>T
NM_016574.3:c.286-179C>T	NP_057658.2:n.286-179C>T
NM_016574.4:c.286-179C>T	NP_057658.2:n.286-179C>T
ENST00000346454.7:c.286-179C>T	ENSP00000278597.5:n.286-179C>T
ENST00000362072.7:c.286-179C>T	ENSP00000354859.3:n.286-179C>T
ENST00000535984.1:n.142-179C>T
ENST00000538967.5:c.286-179C>T	ENSP00000438215.1:n.286-179C>T
ENST00000540600.5:n.351-179C>T
ENST00000542968.5:c.286-179C>T	ENSP00000442172.1:n.286-179C>T
ENST00000543292.1:c.286-179C>T	ENSP00000438419.1:n.286-179C>T
ENST00000544518.5:c.290-186C>T	ENSP00000441068.1:n.290-186C>T
XM_017017296.2:c.286-179C>T	XP_016872785.1:n.286-179C>T