Canonical Allele Identifier: CA597020846
Gene: DRD4 HGNC NCBI

Linked Data

dbSNP Id: rs1335052571
gnomAD v2: 11-640346-G-GT
gnomAD v4: 11-640346-G-GT
MyVariant Identifiers: chr11:g.640346_640347insT (hg19) chr11:g.640346_640347insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.640346_640347insT , CM000673.2:g.640346_640347insT GRCh38
NC_000011.9:g.640346_640347insT , CM000673.1:g.640346_640347insT GRCh37
NC_000011.8:g.630346_630347insT NCBI36
NG_021241.1:g.8042_8043insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000176183.6:c.1057+40_1057+41insT MANE Select ENSP00000176183.5:n.1057+40_1057+41insT
ENST00000176183.5:c.1057+40_1057+41insT ENSP00000176183.5:n.1057+40_1057+41insT
NM_000797.3:c.1057+40_1057+41insT NP_000788.2:n.1057+40_1057+41insT
NM_000797.4:c.1057+40_1057+41insT MANE Select NP_000788.2:n.1057+40_1057+41insT
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