Canonical Allele Identifier: CA2576133129

Gene: ARRB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4719325_4719327del , CM000679.2:g.4719325_4719327del	GRCh38
NC_000017.10:g.4622620_4622622del , CM000679.1:g.4622620_4622622del	GRCh37
NC_000017.9:g.4569369_4569371del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269260.7:c.822_824del MANE Select	ENSP00000269260.2:p.Ile275del
ENST00000269260.6:c.822_824del	ENSP00000269260.2:p.Ile275del
ENST00000346341.6:c.777_779del	ENSP00000341895.2:p.Ile260del
ENST00000381488.10:c.777_779del	ENSP00000370898.6:p.Ile260del
ENST00000412477.7:c.885_887del	ENSP00000403701.3:p.Ile296del
ENST00000571206.1:c.246_248del	ENSP00000460607.1:p.Ile83del
ENST00000571428.5:c.246_248del	ENSP00000465877.1:p.Ile83del
ENST00000572457.5:c.246_248del	ENSP00000465296.1:p.Ile83del
ENST00000574502.5:c.*300_*302del	ENSP00000458371.1:n.*300_*302del
ENST00000574954.5:c.246_248del	ENSP00000466344.1:p.Ile83del
ENST00000575877.5:c.786+36_786+38del	ENSP00000466857.1:n.786+36_786+38del
ENST00000576235.1:c.704_706del	ENSP00000460879.1:n.704_706del
NM_001257328.1:c.885_887del	NP_001244257.1:p.Ile296del
NM_001257329.1:c.786+36_786+38del	NP_001244258.1:n.786+36_786+38del
NM_001257330.1:c.822_824del	NP_001244259.1:p.Ile275del
NM_001257331.1:c.777_779del	NP_001244260.1:p.Ile260del
NM_004313.3:c.822_824del	NP_004304.1:p.Ile275del
NM_199004.1:c.777_779del	NP_945355.1:p.Ile260del
NR_047516.1:n.1019_1021del
XM_006721520.1:c.246_248del	XP_006721583.1:p.Ile83del
XM_006721521.1:c.246_248del	XP_006721584.1:p.Ile83del
XM_011523858.1:c.915_917del	XP_011522160.1:p.Ile306del
XM_011523859.1:c.870_872del	XP_011522161.1:p.Ile291del
NM_001330064.1:c.246_248del	NP_001316993.1:p.Ile83del
XM_011523858.2:c.915_917del	XP_011522160.1:p.Ile306del
XM_017024645.1:c.246_248del	XP_016880134.1:p.Ile83del
XM_024450751.1:c.822_824del	XP_024306519.1:p.Ile275del
XM_024450752.1:c.246_248del	XP_024306520.1:p.Ile83del
XM_024450753.1:c.246_248del	XP_024306521.1:p.Ile83del
XR_002958006.1:n.829_831del
XR_002958007.1:n.829_831del
NM_004313.4:c.822_824del MANE Select	NP_004304.1:p.Ile275del
NM_001257328.2:c.885_887del	NP_001244257.1:p.Ile296del
NM_001257329.2:c.786+36_786+38del	NP_001244258.1:n.786+36_786+38del
NM_001257330.2:c.822_824del	NP_001244259.1:p.Ile275del
NM_001257331.2:c.777_779del	NP_001244260.1:p.Ile260del
NM_001330064.2:c.246_248del	NP_001316993.1:p.Ile83del
NM_199004.2:c.777_779del	NP_945355.1:p.Ile260del
NR_047516.2:n.881_883del