Canonical Allele Identifier: CA2832589399

Gene: DRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113424176G>T , CM000673.2:g.113424176G>T	GRCh38
NC_000011.9:g.113294898G>T , CM000673.1:g.113294898G>T	GRCh37
NC_000011.8:g.112800108G>T	NCBI36
NG_008841.1:g.56104C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000795.4:c.285+191C>A MANE Select	NP_000786.1:n.285+191C>A
ENST00000362072.8:c.285+191C>A MANE Select	ENSP00000354859.3:n.285+191C>A
NM_000795.3:c.285+191C>A	NP_000786.1:n.285+191C>A
NM_016574.3:c.285+191C>A	NP_057658.2:n.285+191C>A
NM_016574.4:c.285+191C>A	NP_057658.2:n.285+191C>A
ENST00000346454.7:c.285+191C>A	ENSP00000278597.5:n.285+191C>A
ENST00000362072.7:c.285+191C>A	ENSP00000354859.3:n.285+191C>A
ENST00000535984.1:n.141+191C>A
ENST00000538967.5:c.285+191C>A	ENSP00000438215.1:n.285+191C>A
ENST00000540600.5:n.350+191C>A
ENST00000542968.5:c.285+191C>A	ENSP00000442172.1:n.285+191C>A
ENST00000543292.1:c.285+191C>A	ENSP00000438419.1:n.285+191C>A
ENST00000544518.5:c.289+187C>A	ENSP00000441068.1:n.289+187C>A
XM_017017296.2:c.285+191C>A	XP_016872785.1:n.285+191C>A