Canonical Allele Identifier: CA597020768
Gene: DRD4 HGNC NCBI

Linked Data

dbSNP Id: rs1564913851
gnomAD v2: 11-640086-GCCCGCCGCGCCCAGCCTCCCCCAGGACCCCTGCGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCCCGGACCCCTGCGGCTCCAACTGTGCT-G
gnomAD v3: 11-640086-GCCCGCCGCGCCCAGCCTCCCCCAGGACCCCTGCGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCCCGGACCCCTGCGGCTCCAACTGTGCT-G
gnomAD v4: 11-640086-GCCCGCCGCGCCCAGCCTCCCCCAGGACCCCTGCGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCCCGGACCCCTGCGGCTCCAACTGTGCT-G
MyVariant Identifiers: chr11:g.640087_640182del (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.640090_640185del , CM000673.2:g.640090_640185del GRCh38
NC_000011.9:g.640090_640185del , CM000673.1:g.640090_640185del GRCh37
NC_000011.8:g.630090_630185del NCBI36
NG_021241.1:g.7786_7881del

Transcript Alleles

HGVS Amino-acid change
ENST00000176183.6:c.841_936del MANE Select ENSP00000176183.5:p.Ala281_Pro312del
ENST00000176183.5:c.841_936del ENSP00000176183.5:p.Ala281_Pro312del
NM_000797.3:c.841_936del NP_000788.2:p.Ala281_Pro312del
NM_000797.4:c.841_936del MANE Select NP_000788.2:p.Ala281_Pro312del
Search 100 bp 5'
Search 100 bp 3'