Canonical Allele Identifier: CA5785830
Gene: DRD4 HGNC NCBI

Linked Data

dbSNP Id: rs1564913814
ExAC: 11:640065 TCCCTGCGGCCCCGACTGTGCGCCCGCCGCGCCCAGCCTCCCCCAGGACCCCTGCGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCCCGGAC / T
gnomAD v2: 11-640065-TCCCTGCGGCCCCGACTGTGCGCCCGCCGCGCCCAGCCTCCCCCAGGACCCCTGCGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCCCGGAC-T
gnomAD v3: 11-640065-TCCCTGCGGCCCCGACTGTGCGCCCGCCGCGCCCAGCCTCCCCCAGGACCCCTGCGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCCCGGAC-T
gnomAD v4: 11-640065-TCCCTGCGGCCCCGACTGTGCGCCCGCCGCGCCCAGCCTCCCCCAGGACCCCTGCGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCCCGGAC-T
MyVariant Identifiers: chr11:g.640066_640161del (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.640075_640170del , CM000673.2:g.640075_640170del GRCh38
NC_000011.9:g.640075_640170del , CM000673.1:g.640075_640170del GRCh37
NC_000011.8:g.630075_630170del NCBI36
NG_021241.1:g.7771_7866del

Transcript Alleles

HGVS Amino-acid change
ENST00000176183.6:c.826_921del MANE Select ENSP00000176183.5:p.Pro276_Gly307del
ENST00000176183.5:c.826_921del ENSP00000176183.5:p.Pro276_Gly307del
NM_000797.3:c.826_921del NP_000788.2:p.Pro276_Gly307del
NM_000797.4:c.826_921del MANE Select NP_000788.2:p.Pro276_Gly307del
Search 100 bp 5'
Search 100 bp 3'