Canonical Allele Identifier: CA545565451

Gene: DRD3

Linked Data

• dbSNP Id: rs61072823
• gnomAD v2: 3-113849273-A-ATTTT
• gnomAD v3: 3-114130426-A-ATTTT
• gnomAD v4: 3-114130426-A-ATTTT
• MyVariant Identifiers: chr3:g.113849275_113849276insTTTT (hg19) ; chr3:g.113849273_113849274insTTTT (hg19) ; chr3:g.114130428_114130429insTTTT (hg38) ; chr3:g.114130426_114130427insTTTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.114130439_114130442dup , CM000665.2:g.114130439_114130442dup	GRCh38
NC_000003.11:g.113849286_113849289dup , CM000665.1:g.113849286_113849289dup	GRCh37
NC_000003.10:g.115331976_115331979dup	NCBI36
NG_008842.2:g.73978_73981dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698213.1:c.*310+688_*310+691dup	ENSP00000513607.1:n.*310+688_*310+691dup
ENST00000383673.5:c.1006+688_1006+691dup MANE Select	ENSP00000373169.2:n.1006+688_1006+691dup
ENST00000295881.9:c.907+688_907+691dup	ENSP00000295881.6:n.907+688_907+691dup
ENST00000383673.4:c.1006+688_1006+691dup	ENSP00000373169.2:n.1006+688_1006+691dup
ENST00000460779.5:c.1006+688_1006+691dup	ENSP00000419402.1:n.1006+688_1006+691dup
ENST00000467632.5:c.1006+688_1006+691dup	ENSP00000420662.1:n.1006+688_1006+691dup
NM_000796.5:c.1006+688_1006+691dup	NP_000787.2:n.1006+688_1006+691dup
NM_001282563.2:c.1006+688_1006+691dup	NP_001269492.1:n.1006+688_1006+691dup
NM_001290809.1:c.1006+688_1006+691dup	NP_001277738.1:n.1006+688_1006+691dup
NM_033663.5:c.907+688_907+691dup	NP_387512.3:n.907+688_907+691dup
XM_011512510.1:c.1006+688_1006+691dup	XP_011510812.1:n.1006+688_1006+691dup
XM_011512511.1:c.1006+688_1006+691dup	XP_011510813.1:n.1006+688_1006+691dup
XM_011512512.1:c.1006+688_1006+691dup	XP_011510814.1:n.1006+688_1006+691dup
XM_017005829.1:c.1006+688_1006+691dup	XP_016861318.1:n.1006+688_1006+691dup
NM_000796.6:c.1006+688_1006+691dup MANE Select	NP_000787.2:n.1006+688_1006+691dup
NM_033663.6:c.907+688_907+691dup	NP_387512.3:n.907+688_907+691dup