Canonical Allele Identifier: CA5785921
Gene: DRD4 HGNC NCBI

Linked Data

dbSNP Id: rs757585485
ExAC: 11:640344 G / GT
gnomAD v2: 11-640344-G-GT
gnomAD v3: 11-640344-G-GT
gnomAD v4: 11-640344-G-GT
MyVariant Identifiers: chr11:g.640344_640345insT (hg19) chr11:g.640344_640345insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.640344_640345insT , CM000673.2:g.640344_640345insT GRCh38
NC_000011.9:g.640344_640345insT , CM000673.1:g.640344_640345insT GRCh37
NC_000011.8:g.630344_630345insT NCBI36
NG_021241.1:g.8040_8041insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000176183.6:c.1057+38_1057+39insT MANE Select ENSP00000176183.5:n.1057+38_1057+39insT
ENST00000176183.5:c.1057+38_1057+39insT ENSP00000176183.5:n.1057+38_1057+39insT
NM_000797.3:c.1057+38_1057+39insT NP_000788.2:n.1057+38_1057+39insT
NM_000797.4:c.1057+38_1057+39insT MANE Select NP_000788.2:n.1057+38_1057+39insT
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