Canonical Allele Identifier: CA2582342931

Gene: STAG2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.124086715dup , CM000685.2:g.124086715dup	GRCh38
NC_000023.10:g.123220565dup , CM000685.1:g.123220565dup	GRCh37
NC_000023.9:g.123048246dup	NCBI36
NG_033796.2:g.131156dup , LRG_782:g.131156dup

Transcript Alleles

HGVS	Amino-acid Change
NM_001042750.2:c.3222dup MANE Select	NP_001036215.1:p.Ser1075IlefsTer12
ENST00000371145.8:c.3222dup MANE Select	ENSP00000360187.4:p.Ser1075IlefsTer12
NM_001042749.2:c.3222dup , LRG_782t1:c.3222dup	NP_001036214.1:p.Ser1075IlefsTer12
NM_001042750.1:c.3222dup , LRG_782t2:c.3222dup	NP_001036215.1:p.Ser1075IlefsTer12
NM_001042751.1:c.3222dup	NP_001036216.1:p.Ser1075IlefsTer12
NM_001042751.2:c.3222dup	NP_001036216.1:p.Ser1075IlefsTer12
NM_001282418.1:c.3222dup , LRG_782t3:c.3222dup	NP_001269347.1:p.Ser1075IlefsTer12
NM_001282418.2:c.3222dup	NP_001269347.1:p.Ser1075IlefsTer12
NM_001375366.1:c.3222dup	NP_001362295.1:p.Ser1075IlefsTer12
NM_001375367.1:c.3222dup	NP_001362296.1:p.Ser1075IlefsTer12
NM_001375368.1:c.3222dup	NP_001362297.1:p.Ser1075IlefsTer12
NM_001375369.1:c.3222dup	NP_001362298.1:p.Ser1075IlefsTer12
NM_001375370.1:c.3222dup	NP_001362299.1:p.Ser1075IlefsTer12
NM_001375371.1:c.3222dup	NP_001362300.1:p.Ser1075IlefsTer12
NM_001375372.1:c.3222dup	NP_001362301.1:p.Ser1075IlefsTer12
NM_001375373.1:c.3222dup	NP_001362302.1:p.Ser1075IlefsTer12
NM_001375374.1:c.3222dup	NP_001362303.1:p.Ser1075IlefsTer12
NM_001375375.1:c.3222dup	NP_001362304.1:p.Ser1075IlefsTer12
NM_001375376.1:c.3222dup	NP_001362305.1:p.Ser1075IlefsTer12
NM_001375377.1:c.3222dup	NP_001362306.1:p.Ser1075IlefsTer12
NM_006603.4:c.3222dup	NP_006594.3:p.Ser1075IlefsTer12
NM_006603.5:c.3222dup	NP_006594.3:p.Ser1075IlefsTer12
ENST00000218089.13:c.3222dup	ENSP00000218089.9:p.Ser1075IlefsTer12
ENST00000371144.7:c.3222dup	ENSP00000360186.3:p.Ser1075IlefsTer12
ENST00000371145.7:c.3222dup	ENSP00000360187.3:p.Ser1075IlefsTer12
ENST00000371157.7:c.3222dup	ENSP00000360199.3:p.Ser1075IlefsTer12
ENST00000371160.5:c.3222dup	ENSP00000360202.1:p.Ser1075IlefsTer12
ENST00000455404.6:c.3222dup	ENSP00000397265.2:p.Ser1075IlefsTer12
ENST00000469481.1:n.453+82968dup
ENST00000686127.1:c.*2020dup	ENSP00000510375.1:n.*2020dup
ENST00000687852.1:c.3222dup	ENSP00000509048.1:p.Ser1075IlefsTer12
ENST00000691035.1:n.3458dup
ENST00000692982.1:c.3222dup	ENSP00000509476.1:p.Ser1075IlefsTer12
ENST00000693144.1:n.4511dup
XM_005262357.1:c.3222dup	XP_005262414.1:p.Ser1075IlefsTer12
XM_005262357.3:c.3222dup	XP_005262414.1:p.Ser1075IlefsTer12
XM_005262358.1:c.3222dup	XP_005262415.1:p.Ser1075IlefsTer12
XM_005262358.2:c.3222dup	XP_005262415.1:p.Ser1075IlefsTer12
XM_005262359.2:c.3222dup	XP_005262416.1:p.Ser1075IlefsTer12
XM_005262359.4:c.3222dup	XP_005262416.1:p.Ser1075IlefsTer12
XM_005262360.1:c.3222dup	XP_005262417.1:p.Ser1075IlefsTer12
XM_005262360.2:c.3222dup	XP_005262417.1:p.Ser1075IlefsTer12
XM_005262361.1:c.3222dup	XP_005262418.1:p.Ser1075IlefsTer12
XM_005262361.2:c.3222dup	XP_005262418.1:p.Ser1075IlefsTer12
XM_006724727.1:c.3222dup	XP_006724790.1:p.Ser1075IlefsTer12
XM_006724728.2:c.3015dup	XP_006724791.1:p.Ser1006IlefsTer12
XM_006724728.4:c.3015dup	XP_006724791.1:p.Ser1006IlefsTer12
XM_011531253.1:c.3222dup	XP_011529555.1:p.Ser1075IlefsTer12
XM_011531253.2:c.3222dup	XP_011529555.1:p.Ser1075IlefsTer12
XM_011531254.1:c.3222dup	XP_011529556.1:p.Ser1075IlefsTer12
XM_017029232.1:c.3222dup	XP_016884721.1:p.Ser1075IlefsTer12
XM_017029233.1:c.3222dup	XP_016884722.1:p.Ser1075IlefsTer12
XM_017029234.1:c.3222dup	XP_016884723.1:p.Ser1075IlefsTer12
XM_017029235.1:c.3015dup	XP_016884724.1:p.Ser1006IlefsTer12
XM_024452326.1:c.3222dup	XP_024308094.1:p.Ser1075IlefsTer12
XM_024452327.1:c.3222dup	XP_024308095.1:p.Ser1075IlefsTer12
XM_024452328.1:c.3222dup	XP_024308096.1:p.Ser1075IlefsTer12
XM_024452329.1:c.3222dup	XP_024308097.1:p.Ser1075IlefsTer12