Canonical Allele Identifier: CA2322735053
Gene: SMARCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11041310A= , CM000681.2:g.11041310A= GRCh38
NC_000019.9:g.11151986A= , CM000681.1:g.11151986A= GRCh37
NC_000019.8:g.11012986A= NCBI36
NG_011556.2:g.85389A=
NG_011556.3:g.85379A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000711079.1:c.4270A= ENSP00000518564.1:p.Ile1424=
ENST00000704344.1:c.4174A= ENSP00000515855.1:p.Ile1392=
ENST00000646693.2:c.4270A= MANE Plus Clinical ENSP00000495368.1:p.Ile1424=
ENST00000344626.10:c.4174A= MANE Select ENSP00000343896.4:p.Ile1392=
ENST00000429416.8:c.4174A= ENSP00000395654.1:p.Ile1392=
ENST00000444061.8:c.4075A= ENSP00000392837.2:p.Ile1359=
ENST00000538456.4:c.341A=
ENST00000586985.2:c.301A= ENSP00000467796.2:p.Ile101=
ENST00000590574.6:c.4075A= ENSP00000466963.1:p.Ile1359=
ENST00000592158.2:c.115A= ENSP00000467200.2:p.Ile39=
ENST00000592604.6:n.2415A=
ENST00000642350.1:c.2668A= ENSP00000495355.1:p.Ile890=
ENST00000642508.1:c.1631A=
ENST00000642628.1:c.4171A= ENSP00000496498.1:p.Ile1391=
ENST00000642726.1:c.4171A= ENSP00000494353.1:p.Ile1391=
ENST00000643208.1:c.2731A= ENSP00000496074.1:p.Ile911=
ENST00000643296.1:c.4084A= ENSP00000496635.1:p.Ile1362=
ENST00000643534.1:c.2459A=
ENST00000643549.1:c.4180A= ENSP00000493975.1:p.Ile1394=
ENST00000643857.1:c.2538A=
ENST00000643929.1:n.667A=
ENST00000643995.1:c.3597A=
ENST00000644065.1:c.2811A=
ENST00000644327.1:c.2846A=
ENST00000644737.1:c.4084A= ENSP00000495548.1:p.Ile1362=
ENST00000644963.1:c.2828A=
ENST00000645061.1:c.2662A= ENSP00000493690.1:p.Ile888=
ENST00000645236.1:c.723A=
ENST00000645460.1:c.4075A= ENSP00000494463.1:p.Ile1359=
ENST00000645648.1:c.2085A= ENSP00000493521.1:n.2085A=
ENST00000646183.1:c.2517A=
ENST00000646484.1:c.4075A= ENSP00000495536.1:p.Ile1359=
ENST00000646510.1:c.4075A= ENSP00000494772.1:p.Ile1359=
ENST00000646593.1:c.2022A= ENSP00000494341.1:n.2022A=
ENST00000646693.1:c.4270A= ENSP00000495368.1:p.Ile1424=
ENST00000646746.1:c.2474A=
ENST00000646889.1:n.677A=
ENST00000647230.1:c.4075A= ENSP00000494676.1:p.Ile1359=
ENST00000647268.1:c.2428A= ENSP00000496176.1:p.Ile810=
ENST00000344626.8:c.4174A= ENSP00000343896.4:p.Ile1392=
ENST00000413806.7:c.4276A= ENSP00000414727.3:p.Ile1426=
ENST00000429416.7:c.4174A= ENSP00000395654.1:p.Ile1392=
ENST00000444061.7:c.4075A= ENSP00000392837.2:p.Ile1359=
ENST00000450717.7:c.4270A= ENSP00000397783.3:p.Ile1424=
ENST00000538456.3:n.488A=
ENST00000541122.6:c.4084A= ENSP00000445036.2:p.Ile1362=
ENST00000585799.5:n.2612A=
ENST00000589677.5:c.4084A= ENSP00000464778.1:p.Ile1362=
ENST00000590574.5:c.4075A= ENSP00000466963.1:p.Ile1359=
ENST00000591595.5:n.2147A=
ENST00000592158.1:c.253A= ENSP00000467200.1:p.Ile85=
ENST00000592604.5:n.1997A=
NM_001128844.1:c.4174A= NP_001122316.1:p.Ile1392=
NM_001128845.1:c.4084A= NP_001122317.1:p.Ile1362=
NM_001128846.1:c.4084A= NP_001122318.1:p.Ile1362=
NM_001128847.1:c.4075A= NP_001122319.1:p.Ile1359=
NM_001128848.1:c.4075A= NP_001122320.1:p.Ile1359=
NM_001128849.1:c.4270A= NP_001122321.1:p.Ile1424=
NM_003072.3:c.4174A= NP_003063.2:p.Ile1392=
XM_005260028.2:c.4183A= XP_005260085.1:p.Ile1395=
XM_005260030.2:c.4171A= XP_005260087.1:p.Ile1391=
XM_005260031.2:c.4174A= XP_005260088.1:p.Ile1392=
XM_005260032.2:c.4084A= XP_005260089.1:p.Ile1362=
XM_005260033.2:c.4084A= XP_005260090.1:p.Ile1362=
XM_005260034.2:c.4075A= XP_005260091.1:p.Ile1359=
XM_005260035.2:c.4075A= XP_005260092.1:p.Ile1359=
XM_006722845.2:c.4270A= XP_006722908.1:p.Ile1424=
XM_006722846.2:c.4270A= XP_006722909.1:p.Ile1424=
XM_006722847.2:c.4270A= XP_006722910.1:p.Ile1424=
XM_011528198.1:c.4270A= XP_011526500.1:p.Ile1424=
XM_024451658.1:c.4270A= XP_024307426.1:p.Ile1424=
XM_024451659.1:c.4270A= XP_024307427.1:p.Ile1424=
XM_024451660.1:c.4183A= XP_024307428.1:p.Ile1395=
XM_024451661.1:c.4171A= XP_024307429.1:p.Ile1391=
XM_024451662.1:c.4174A= XP_024307430.1:p.Ile1392=
XM_024451663.1:c.4171A= XP_024307431.1:p.Ile1391=
XM_024451664.1:c.4084A= XP_024307432.1:p.Ile1362=
XM_024451665.1:c.4084A= XP_024307433.1:p.Ile1362=
XM_024451666.1:c.4075A= XP_024307434.1:p.Ile1359=
XM_024451667.1:c.4075A= XP_024307435.1:p.Ile1359=
NM_001128844.3:c.4174A= NP_001122316.1:p.Ile1392=
NM_001128845.2:c.4084A= NP_001122317.1:p.Ile1362=
NM_001128846.2:c.4084A= NP_001122318.1:p.Ile1362=
NM_001128847.4:c.4075A= NP_001122319.1:p.Ile1359=
NM_001128848.2:c.4075A= NP_001122320.1:p.Ile1359=
NM_001128849.3:c.4270A= NP_001122321.1:p.Ile1424=
NM_001374457.1:c.4075A= NP_001361386.1:p.Ile1359=
NM_003072.5:c.4174A= MANE Select NP_003063.2:p.Ile1392=
NR_164683.1:n.4564A=
NM_001387283.1:c.4270A= MANE Plus Clinical NP_001374212.1:p.Ile1424=