Canonical Allele Identifier: CA2322734980

Gene: SMARCA4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11041428G= , CM000681.2:g.11041428G=	GRCh38
NC_000019.9:g.11152104G= , CM000681.1:g.11152104G=	GRCh37
NC_000019.8:g.11013104G=	NCBI36
NG_011556.2:g.85507G=
NG_011556.3:g.85497G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000711079.1:c.4388G=	ENSP00000518564.1:p.Arg1463=
ENST00000704344.1:c.4292G=	ENSP00000515855.1:p.Arg1431=
ENST00000646693.2:c.4388G= MANE Plus Clinical	ENSP00000495368.1:p.Arg1463=
ENST00000344626.10:c.4292G= MANE Select	ENSP00000343896.4:p.Arg1431=
ENST00000429416.8:c.4292G=	ENSP00000395654.1:p.Arg1431=
ENST00000444061.8:c.4193G=	ENSP00000392837.2:p.Arg1398=
ENST00000538456.4:c.459G=
ENST00000586985.2:c.419G=	ENSP00000467796.2:p.Arg140=
ENST00000590574.6:c.4193G=	ENSP00000466963.1:p.Arg1398=
ENST00000592158.2:c.233G=	ENSP00000467200.2:p.Arg78=
ENST00000592604.6:n.2533G=
ENST00000642350.1:c.2786G=	ENSP00000495355.1:p.Arg929=
ENST00000642508.1:c.1749G=
ENST00000642628.1:c.4289G=	ENSP00000496498.1:p.Arg1430=
ENST00000642726.1:c.4289G=	ENSP00000494353.1:p.Arg1430=
ENST00000643208.1:c.2849G=	ENSP00000496074.1:p.Arg950=
ENST00000643296.1:c.4202G=	ENSP00000496635.1:p.Arg1401=
ENST00000643534.1:c.2577G=
ENST00000643549.1:c.4298G=	ENSP00000493975.1:p.Arg1433=
ENST00000643857.1:c.2656G=
ENST00000643929.1:n.785G=
ENST00000643995.1:c.3715G=
ENST00000644065.1:c.2929G=
ENST00000644327.1:c.2964G=
ENST00000644737.1:c.4202G=	ENSP00000495548.1:p.Arg1401=
ENST00000644963.1:c.2946G=
ENST00000645061.1:c.2780G=	ENSP00000493690.1:p.Arg927=
ENST00000645236.1:c.841G=
ENST00000645460.1:c.4193G=	ENSP00000494463.1:p.Arg1398=
ENST00000645648.1:c.2203G=	ENSP00000493521.1:n.2203G=
ENST00000646183.1:c.2635G=
ENST00000646484.1:c.4193G=	ENSP00000495536.1:p.Arg1398=
ENST00000646510.1:c.4193G=	ENSP00000494772.1:p.Arg1398=
ENST00000646593.1:c.2140G=	ENSP00000494341.1:n.2140G=
ENST00000646693.1:c.4388G=	ENSP00000495368.1:p.Arg1463=
ENST00000646746.1:c.2592G=
ENST00000646889.1:n.795G=
ENST00000647230.1:c.4193G=	ENSP00000494676.1:p.Arg1398=
ENST00000647268.1:c.2546G=	ENSP00000496176.1:p.Arg849=
ENST00000344626.8:c.4292G=	ENSP00000343896.4:p.Arg1431=
ENST00000413806.7:c.4394G=	ENSP00000414727.3:p.Arg1465=
ENST00000429416.7:c.4292G=	ENSP00000395654.1:p.Arg1431=
ENST00000444061.7:c.4193G=	ENSP00000392837.2:p.Arg1398=
ENST00000450717.7:c.4388G=	ENSP00000397783.3:p.Arg1463=
ENST00000538456.3:n.606G=
ENST00000541122.6:c.4202G=	ENSP00000445036.2:p.Arg1401=
ENST00000585799.5:n.2730G=
ENST00000589677.5:c.4202G=	ENSP00000464778.1:p.Arg1401=
ENST00000590574.5:c.4193G=	ENSP00000466963.1:p.Arg1398=
ENST00000591595.5:n.2265G=
ENST00000592158.1:c.371G=	ENSP00000467200.1:p.Arg124=
ENST00000592604.5:n.2115G=
NM_001128844.1:c.4292G=	NP_001122316.1:p.Arg1431=
NM_001128845.1:c.4202G=	NP_001122317.1:p.Arg1401=
NM_001128846.1:c.4202G=	NP_001122318.1:p.Arg1401=
NM_001128847.1:c.4193G=	NP_001122319.1:p.Arg1398=
NM_001128848.1:c.4193G=	NP_001122320.1:p.Arg1398=
NM_001128849.1:c.4388G=	NP_001122321.1:p.Arg1463=
NM_003072.3:c.4292G=	NP_003063.2:p.Arg1431=
XM_005260028.2:c.4301G=	XP_005260085.1:p.Arg1434=
XM_005260030.2:c.4289G=	XP_005260087.1:p.Arg1430=
XM_005260031.2:c.4292G=	XP_005260088.1:p.Arg1431=
XM_005260032.2:c.4202G=	XP_005260089.1:p.Arg1401=
XM_005260033.2:c.4202G=	XP_005260090.1:p.Arg1401=
XM_005260034.2:c.4193G=	XP_005260091.1:p.Arg1398=
XM_005260035.2:c.4193G=	XP_005260092.1:p.Arg1398=
XM_006722845.2:c.4388G=	XP_006722908.1:p.Arg1463=
XM_006722846.2:c.4388G=	XP_006722909.1:p.Arg1463=
XM_006722847.2:c.4388G=	XP_006722910.1:p.Arg1463=
XM_011528198.1:c.4388G=	XP_011526500.1:p.Arg1463=
XM_024451658.1:c.4388G=	XP_024307426.1:p.Arg1463=
XM_024451659.1:c.4388G=	XP_024307427.1:p.Arg1463=
XM_024451660.1:c.4301G=	XP_024307428.1:p.Arg1434=
XM_024451661.1:c.4289G=	XP_024307429.1:p.Arg1430=
XM_024451662.1:c.4292G=	XP_024307430.1:p.Arg1431=
XM_024451663.1:c.4289G=	XP_024307431.1:p.Arg1430=
XM_024451664.1:c.4202G=	XP_024307432.1:p.Arg1401=
XM_024451665.1:c.4202G=	XP_024307433.1:p.Arg1401=
XM_024451666.1:c.4193G=	XP_024307434.1:p.Arg1398=
XM_024451667.1:c.4193G=	XP_024307435.1:p.Arg1398=
NM_001128844.3:c.4292G=	NP_001122316.1:p.Arg1431=
NM_001128845.2:c.4202G=	NP_001122317.1:p.Arg1401=
NM_001128846.2:c.4202G=	NP_001122318.1:p.Arg1401=
NM_001128847.4:c.4193G=	NP_001122319.1:p.Arg1398=
NM_001128848.2:c.4193G=	NP_001122320.1:p.Arg1398=
NM_001128849.3:c.4388G=	NP_001122321.1:p.Arg1463=
NM_001374457.1:c.4193G=	NP_001361386.1:p.Arg1398=
NM_003072.5:c.4292G= MANE Select	NP_003063.2:p.Arg1431=
NR_164683.1:n.4682G=
NM_001387283.1:c.4388G= MANE Plus Clinical	NP_001374212.1:p.Arg1463=