Canonical Allele Identifier: CA2001161861

Gene: DRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113442666_113442667delinsCT , CM000673.2:g.113442666_113442667delinsCT	GRCh38
NC_000011.9:g.113313388_113313389delinsCT , CM000673.1:g.113313388_113313389delinsCT	GRCh37
NC_000011.8:g.112818598_112818599delinsCT	NCBI36
NG_008841.1:g.37613_37614delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.-31-17985_-31-17984delinsAG MANE Select	ENSP00000354859.3:n.-31-17985_-31-17984delinsAG
ENST00000346454.7:c.-31-17985_-31-17984delinsAG	ENSP00000278597.5:n.-31-17985_-31-17984delinsAG
ENST00000362072.7:c.-31-17985_-31-17984delinsAG	ENSP00000354859.3:n.-31-17985_-31-17984delinsAG
ENST00000540600.5:n.35-17985_35-17984delinsAG
ENST00000542616.1:c.-31-17985_-31-17984delinsAG	ENSP00000441474.1:n.-31-17985_-31-17984delinsAG
ENST00000543292.1:c.-32+4904_-32+4905delinsAG	ENSP00000438419.1:n.-32+4904_-32+4905delinsAG
NM_000795.3:c.-31-17985_-31-17984delinsAG	NP_000786.1:n.-31-17985_-31-17984delinsAG
NM_016574.3:c.-31-17985_-31-17984delinsAG	NP_057658.2:n.-31-17985_-31-17984delinsAG
XM_017017296.2:c.-31-17985_-31-17984delinsAG	XP_016872785.1:n.-31-17985_-31-17984delinsAG
NM_000795.4:c.-31-17985_-31-17984delinsAG MANE Select	NP_000786.1:n.-31-17985_-31-17984delinsAG
NM_016574.4:c.-31-17985_-31-17984delinsAG	NP_057658.2:n.-31-17985_-31-17984delinsAG