Canonical Allele Identifier: CA2001167995
Gene: DRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113412747_113412750delinsTGGA , CM000673.2:g.113412747_113412750delinsTGGA GRCh38
NC_000011.9:g.113283469_113283472delinsTGGA , CM000673.1:g.113283469_113283472delinsTGGA GRCh37
NC_000011.8:g.112788679_112788682delinsTGGA NCBI36
NG_008841.1:g.67530_67533delinsTCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.944_947delinsTCCA MANE Select ENSP00000354859.3:p.Leu315=
ENST00000346454.7:c.857_860delinsTCCA ENSP00000278597.5:p.Leu286=
ENST00000362072.7:c.944_947delinsTCCA ENSP00000354859.3:p.Leu315=
ENST00000538967.5:c.950_953delinsTCCA ENSP00000438215.1:p.Leu317=
ENST00000542968.5:c.944_947delinsTCCA ENSP00000442172.1:p.Leu315=
ENST00000544518.5:c.941_944delinsTCCA ENSP00000441068.1:p.Leu314=
NM_000795.3:c.944_947delinsTCCA NP_000786.1:p.Leu315=
NM_016574.3:c.857_860delinsTCCA NP_057658.2:p.Leu286=
XM_017017296.2:c.944_947delinsTCCA XP_016872785.1:p.Leu315=
NM_000795.4:c.944_947delinsTCCA MANE Select NP_000786.1:p.Leu315=
NM_016574.4:c.857_860delinsTCCA NP_057658.2:p.Leu286=