Canonical Allele Identifier: CA1052367008
Gene: DRD3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.114130431_114130432insCTT , CM000665.2:g.114130431_114130432insCTT GRCh38
NC_000003.11:g.113849278_113849279insCTT , CM000665.1:g.113849278_113849279insCTT GRCh37
NC_000003.10:g.115331968_115331969insCTT NCBI36
NG_008842.2:g.73978_73979insGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000698213.1:c.*310+688_*310+689insGAA ENSP00000513607.1:n.*310+688_*310+689insGAA
ENST00000383673.5:c.1006+688_1006+689insGAA MANE Select ENSP00000373169.2:n.1006+688_1006+689insGAA
ENST00000295881.9:c.907+688_907+689insGAA ENSP00000295881.6:n.907+688_907+689insGAA
ENST00000383673.4:c.1006+688_1006+689insGAA ENSP00000373169.2:n.1006+688_1006+689insGAA
ENST00000460779.5:c.1006+688_1006+689insGAA ENSP00000419402.1:n.1006+688_1006+689insGAA
ENST00000467632.5:c.1006+688_1006+689insGAA ENSP00000420662.1:n.1006+688_1006+689insGAA
NM_000796.5:c.1006+688_1006+689insGAA NP_000787.2:n.1006+688_1006+689insGAA
NM_001282563.2:c.1006+688_1006+689insGAA NP_001269492.1:n.1006+688_1006+689insGAA
NM_001290809.1:c.1006+688_1006+689insGAA NP_001277738.1:n.1006+688_1006+689insGAA
NM_033663.5:c.907+688_907+689insGAA NP_387512.3:n.907+688_907+689insGAA
XM_011512510.1:c.1006+688_1006+689insGAA XP_011510812.1:n.1006+688_1006+689insGAA
XM_011512511.1:c.1006+688_1006+689insGAA XP_011510813.1:n.1006+688_1006+689insGAA
XM_011512512.1:c.1006+688_1006+689insGAA XP_011510814.1:n.1006+688_1006+689insGAA
XM_017005829.1:c.1006+688_1006+689insGAA XP_016861318.1:n.1006+688_1006+689insGAA
NM_000796.6:c.1006+688_1006+689insGAA MANE Select NP_000787.2:n.1006+688_1006+689insGAA
NM_033663.6:c.907+688_907+689insGAA NP_387512.3:n.907+688_907+689insGAA