Canonical Allele Identifier: CA597020783
Gene: DRD4 HGNC NCBI

Linked Data

dbSNP Id: rs1858189855
gnomAD v2: 11-640119-C-CGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCCAGGACCCCTGT
gnomAD v3: 11-640119-C-CGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCCAGGACCCCTGT
gnomAD v4: 11-640119-C-CGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCCAGGACCCCTGT
MyVariant Identifiers: chr11:g.640119_640120insGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCCAGGACCCCTGT (hg19) chr11:g.640119_640120insGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCCAGGACCCCTGT (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.640156_640157insAGGACCCCTGTGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCC , CM000673.2:g.640156_640157insAGGACCCCTGTGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCC GRCh38
NC_000011.9:g.640156_640157insAGGACCCCTGTGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCC , CM000673.1:g.640156_640157insAGGACCCCTGTGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCC GRCh37
NC_000011.8:g.630156_630157insAGGACCCCTGTGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCC NCBI36
NG_021241.1:g.7852_7853insAGGACCCCTGTGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCC

Transcript Alleles

HGVS Amino-acid change
ENST00000176183.6:c.907_908insAGGACCCCTGTGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCC MANE Select ENSP00000176183.5:p.Pro302_Pro303insGlnAs...
ENST00000176183.5:c.907_908insAGGACCCCTGTGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCC ENSP00000176183.5:p.Pro302_Pro303insGlnAs...
NM_000797.3:c.907_908insAGGACCCCTGTGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCC NP_000788.2:p.Pro302_Pro303insGlnAspProCy...
NM_000797.4:c.907_908insAGGACCCCTGTGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCC MANE Select NP_000788.2:p.Pro302_Pro303insGlnAspProCy...
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