Canonical Allele Identifier: CA2703942580
Gene: DRD3 HGNC NCBI

Linked Data

dbSNP Id: rs2107827422

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.114130425dup , CM000665.2:g.114130425dup GRCh38
NC_000003.11:g.113849272dup , CM000665.1:g.113849272dup GRCh37
NC_000003.10:g.115331962dup NCBI36
NG_008842.2:g.73983dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000698213.1:c.*310+693dup ENSP00000513607.1:n.*310+693dup
ENST00000383673.5:c.1006+693dup MANE Select ENSP00000373169.2:n.1006+693dup
ENST00000295881.9:c.907+693dup ENSP00000295881.6:n.907+693dup
ENST00000383673.4:c.1006+693dup ENSP00000373169.2:n.1006+693dup
ENST00000460779.5:c.1006+693dup ENSP00000419402.1:n.1006+693dup
ENST00000467632.5:c.1006+693dup ENSP00000420662.1:n.1006+693dup
NM_000796.5:c.1006+693dup NP_000787.2:n.1006+693dup
NM_001282563.2:c.1006+693dup NP_001269492.1:n.1006+693dup
NM_001290809.1:c.1006+693dup NP_001277738.1:n.1006+693dup
NM_033663.5:c.907+693dup NP_387512.3:n.907+693dup
XM_011512510.1:c.1006+693dup XP_011510812.1:n.1006+693dup
XM_011512511.1:c.1006+693dup XP_011510813.1:n.1006+693dup
XM_011512512.1:c.1006+693dup XP_011510814.1:n.1006+693dup
XM_017005829.1:c.1006+693dup XP_016861318.1:n.1006+693dup
NM_000796.6:c.1006+693dup MANE Select NP_000787.2:n.1006+693dup
NM_033663.6:c.907+693dup NP_387512.3:n.907+693dup