Canonical Allele Identifier: CA597020765
Gene: DRD4 HGNC NCBI

Linked Data

dbSNP Id: rs1564913839
gnomAD v2: 11-640079-ACTGTGCGCCCGCCGCGCCCAGCCTCCCCCAGGACCCCTGCGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCCC-A
gnomAD v3: 11-640079-ACTGTGCGCCCGCCGCGCCCAGCCTCCCCCAGGACCCCTGCGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCCC-A
gnomAD v4: 11-640079-ACTGTGCGCCCGCCGCGCCCAGCCTCCCCCAGGACCCCTGCGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCCC-A
MyVariant Identifiers: chr11:g.640080_640157del (hg19) chr11:g.640080_640157del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.640080_640157del , CM000673.2:g.640080_640157del GRCh38
NC_000011.9:g.640080_640157del , CM000673.1:g.640080_640157del GRCh37
NC_000011.8:g.630080_630157del NCBI36
NG_021241.1:g.7776_7853del

Transcript Alleles

HGVS Amino-acid change
ENST00000176183.6:c.831_908del MANE Select ENSP00000176183.5:p.Asp277_Pro303delinsGl...
ENST00000176183.5:c.831_908del ENSP00000176183.5:p.Asp277_Pro303delinsGl...
NM_000797.3:c.831_908del NP_000788.2:p.Asp277_Pro303delinsGlu
NM_000797.4:c.831_908del MANE Select NP_000788.2:p.Asp277_Pro303delinsGlu
Search 100 bp 5'
Search 100 bp 3'