Canonical Allele Identifier: CA897332709

Gene: DRD3

Linked Data

• dbSNP Id: rs1285095626
• gnomAD v3: 3-114172052-TA-T
• gnomAD v4: 3-114172052-TA-T
• MyVariant Identifiers: chr3:g.113890900del (hg19) ; chr3:g.114172053del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.114172054del , CM000665.2:g.114172054del	GRCh38
NC_000003.11:g.113890901del , CM000665.1:g.113890901del	GRCh37
NC_000003.10:g.115373591del	NCBI36
NG_008842.2:g.32355del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698213.1:c.-35-26del	ENSP00000513607.1:n.-35-26del
ENST00000383673.5:c.-35-26del MANE Select	ENSP00000373169.2:n.-35-26del
ENST00000295881.9:c.-35-26del	ENSP00000295881.6:n.-35-26del
ENST00000383673.4:c.-35-26del	ENSP00000373169.2:n.-35-26del
ENST00000460779.5:c.-35-26del	ENSP00000419402.1:n.-35-26del
ENST00000467632.5:c.-35-26del	ENSP00000420662.1:n.-35-26del
NM_000796.5:c.-35-26del	NP_000787.2:n.-35-26del
NM_001282563.2:c.-35-26del	NP_001269492.1:n.-35-26del
NM_001290809.1:c.-35-26del	NP_001277738.1:n.-35-26del
NM_033663.5:c.-35-26del	NP_387512.3:n.-35-26del
XM_011512510.1:c.-35-26del	XP_011510812.1:n.-35-26del
XM_011512511.1:c.-35-26del	XP_011510813.1:n.-35-26del
XM_011512512.1:c.-35-26del	XP_011510814.1:n.-35-26del
XM_017005829.1:c.-35-26del	XP_016861318.1:n.-35-26del
NM_000796.6:c.-35-26del MANE Select	NP_000787.2:n.-35-26del
NM_033663.6:c.-35-26del	NP_387512.3:n.-35-26del