Canonical Allele Identifier: CA2244519294
Gene: ARRB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4719258_4719260delinsCTT , CM000679.2:g.4719258_4719260delinsCTT GRCh38
NC_000017.10:g.4622553_4622555delinsCTT , CM000679.1:g.4622553_4622555delinsCTT GRCh37
NC_000017.9:g.4569302_4569304delinsCTT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000269260.7:c.780-25_780-23delinsCTT MANE Select ENSP00000269260.2:n.780-25_780-23delinsCT...
ENST00000269260.6:c.780-25_780-23delinsCTT ENSP00000269260.2:n.780-25_780-23delinsCT...
ENST00000346341.6:c.735-25_735-23delinsCTT ENSP00000341895.2:n.735-25_735-23delinsCT...
ENST00000381488.10:c.735-25_735-23delinsCTT ENSP00000370898.6:n.735-25_735-23delinsCT...
ENST00000412477.7:c.843-25_843-23delinsCTT ENSP00000403701.3:n.843-25_843-23delinsCT...
ENST00000571206.1:c.204-25_204-23delinsCTT ENSP00000460607.1:n.204-25_204-23delinsCT...
ENST00000571428.5:c.204-25_204-23delinsCTT ENSP00000465877.1:n.204-25_204-23delinsCT...
ENST00000572457.5:c.204-25_204-23delinsCTT ENSP00000465296.1:n.204-25_204-23delinsCT...
ENST00000574502.5:c.*258-25_*258-23delinsCTT ENSP00000458371.1:n.*258-25_*258-23delins...
ENST00000574954.5:c.204-25_204-23delinsCTT ENSP00000466344.1:n.204-25_204-23delinsCT...
ENST00000575877.5:c.780-25_780-23delinsCTT ENSP00000466857.1:n.780-25_780-23delinsCT...
ENST00000576235.1:c.662-25_662-23delinsCTT ENSP00000460879.1:n.662-25_662-23delinsCT...
NM_001257328.1:c.843-25_843-23delinsCTT NP_001244257.1:n.843-25_843-23delinsCTT
NM_001257329.1:c.780-25_780-23delinsCTT NP_001244258.1:n.780-25_780-23delinsCTT
NM_001257330.1:c.780-25_780-23delinsCTT NP_001244259.1:n.780-25_780-23delinsCTT
NM_001257331.1:c.735-25_735-23delinsCTT NP_001244260.1:n.735-25_735-23delinsCTT
NM_004313.3:c.780-25_780-23delinsCTT NP_004304.1:n.780-25_780-23delinsCTT
NM_199004.1:c.735-25_735-23delinsCTT NP_945355.1:n.735-25_735-23delinsCTT
NR_047516.1:n.977-25_977-23delinsCTT
XM_006721520.1:c.204-25_204-23delinsCTT XP_006721583.1:n.204-25_204-23delinsCTT
XM_006721521.1:c.204-25_204-23delinsCTT XP_006721584.1:n.204-25_204-23delinsCTT
XM_011523858.1:c.873-25_873-23delinsCTT XP_011522160.1:n.873-25_873-23delinsCTT
XM_011523859.1:c.828-25_828-23delinsCTT XP_011522161.1:n.828-25_828-23delinsCTT
NM_001330064.1:c.204-25_204-23delinsCTT NP_001316993.1:n.204-25_204-23delinsCTT
XM_011523858.2:c.873-25_873-23delinsCTT XP_011522160.1:n.873-25_873-23delinsCTT
XM_017024645.1:c.204-25_204-23delinsCTT XP_016880134.1:n.204-25_204-23delinsCTT
XM_024450751.1:c.780-25_780-23delinsCTT XP_024306519.1:n.780-25_780-23delinsCTT
XM_024450752.1:c.204-25_204-23delinsCTT XP_024306520.1:n.204-25_204-23delinsCTT
XM_024450753.1:c.204-25_204-23delinsCTT XP_024306521.1:n.204-25_204-23delinsCTT
XR_002958006.1:n.787-25_787-23delinsCTT
XR_002958007.1:n.787-25_787-23delinsCTT
NM_004313.4:c.780-25_780-23delinsCTT MANE Select NP_004304.1:n.780-25_780-23delinsCTT
NM_001257328.2:c.843-25_843-23delinsCTT NP_001244257.1:n.843-25_843-23delinsCTT
NM_001257329.2:c.780-25_780-23delinsCTT NP_001244258.1:n.780-25_780-23delinsCTT
NM_001257330.2:c.780-25_780-23delinsCTT NP_001244259.1:n.780-25_780-23delinsCTT
NM_001257331.2:c.735-25_735-23delinsCTT NP_001244260.1:n.735-25_735-23delinsCTT
NM_001330064.2:c.204-25_204-23delinsCTT NP_001316993.1:n.204-25_204-23delinsCTT
NM_199004.2:c.735-25_735-23delinsCTT NP_945355.1:n.735-25_735-23delinsCTT
NR_047516.2:n.839-25_839-23delinsCTT