Canonical Allele Identifier: CA656665265

Gene: ARRB2

Linked Data

• COSMIC: COSN22373209

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4710664_4710665insT , CM000679.2:g.4710664_4710665insT	GRCh38
NC_000017.10:g.4613959_4613960insT , CM000679.1:g.4613959_4613960insT	GRCh37
NC_000017.9:g.4560708_4560709insT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269260.7:c.-58_-57insT MANE Select	ENSP00000269260.2:n.-58_-57insT
ENST00000269260.6:c.-58_-57insT	ENSP00000269260.2:n.-58_-57insT
ENST00000346341.6:c.-58_-57insT	ENSP00000341895.2:n.-58_-57insT
ENST00000570718.5:n.33_34insT
ENST00000570739.5:n.33_34insT
ENST00000572457.5:c.-542_-541insT	ENSP00000465296.1:n.-542_-541insT
ENST00000574502.5:c.-58_-57insT	ENSP00000458371.1:n.-58_-57insT
ENST00000574888.5:n.10_11insT
ENST00000574954.5:c.-603_-602insT	ENSP00000466344.1:n.-603_-602insT
ENST00000575131.5:n.4_5insT
NM_001257328.1:c.-58_-57insT	NP_001244257.1:n.-58_-57insT
NM_001257329.1:c.-58_-57insT	NP_001244258.1:n.-58_-57insT
NM_001257330.1:c.-58_-57insT	NP_001244259.1:n.-58_-57insT
NM_001257331.1:c.-58_-57insT	NP_001244260.1:n.-58_-57insT
NM_004313.3:c.-58_-57insT	NP_004304.1:n.-58_-57insT
NM_199004.1:c.-58_-57insT	NP_945355.1:n.-58_-57insT
NR_047516.1:n.171_172insT
XM_006721520.1:c.-558_-557insT	XP_006721583.1:n.-558_-557insT
NM_001330064.1:c.-558_-557insT	NP_001316993.1:n.-558_-557insT
XM_024450751.1:c.-58_-57insT	XP_024306519.1:n.-58_-57insT
XM_024450752.1:c.-603_-602insT	XP_024306520.1:n.-603_-602insT
XM_024450753.1:c.-558_-557insT	XP_024306521.1:n.-558_-557insT
XR_002958006.1:n.35_36insT
XR_002958007.1:n.35_36insT
NM_004313.4:c.-58_-57insT MANE Select	NP_004304.1:n.-58_-57insT
NM_001257328.2:c.-58_-57insT	NP_001244257.1:n.-58_-57insT
NM_001257329.2:c.-58_-57insT	NP_001244258.1:n.-58_-57insT
NM_001257330.2:c.-58_-57insT	NP_001244259.1:n.-58_-57insT
NM_001257331.2:c.-58_-57insT	NP_001244260.1:n.-58_-57insT
NM_001330064.2:c.-558_-557insT	NP_001316993.1:n.-558_-557insT
NM_199004.2:c.-58_-57insT	NP_945355.1:n.-58_-57insT
NR_047516.2:n.33_34insT