Canonical Allele Identifier: CA679151080
Gene: DRD4 HGNC NCBI

Linked Data

dbSNP Id: rs1460454367
gnomAD v3: 11-640321-TGAGGGGCGGGGAG-T
gnomAD v4: 11-640321-TGAGGGGCGGGGAG-T
MyVariant Identifiers: chr11:g.640322_640334del (hg19) chr11:g.640322_640334del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.640325_640337del , CM000673.2:g.640325_640337del GRCh38
NC_000011.9:g.640325_640337del , CM000673.1:g.640325_640337del GRCh37
NC_000011.8:g.630325_630337del NCBI36
NG_021241.1:g.8021_8033del

Transcript Alleles

HGVS Amino-acid Change
ENST00000176183.6:c.1057+19_1057+31del MANE Select ENSP00000176183.5:n.1057+19_1057+31del
ENST00000176183.5:c.1057+19_1057+31del ENSP00000176183.5:n.1057+19_1057+31del
NM_000797.3:c.1057+19_1057+31del NP_000788.2:n.1057+19_1057+31del
NM_000797.4:c.1057+19_1057+31del MANE Select NP_000788.2:n.1057+19_1057+31del
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