Canonical Allele Identifier: CA2582453118

Gene: SMARCA4

Linked Data

• gnomAD v4: 19-10961134-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10961139del , CM000681.2:g.10961139del	GRCh38
NC_000019.9:g.11071815del , CM000681.1:g.11071815del	GRCh37
NC_000019.8:g.10932815del	NCBI36
NG_011556.2:g.5218del
NG_011556.3:g.5208del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000711079.1:c.-67del	ENSP00000518564.1:n.-67del
ENST00000704344.1:c.-64del	ENSP00000515855.1:n.-64del
ENST00000646693.2:c.-64del MANE Plus Clinical	ENSP00000495368.1:n.-64del
ENST00000344626.10:c.-67del MANE Select	ENSP00000343896.4:n.-67del
ENST00000429416.8:c.-143del	ENSP00000395654.1:n.-143del
ENST00000444061.8:c.-67del	ENSP00000392837.2:n.-67del
ENST00000642628.1:c.-67del	ENSP00000496498.1:n.-67del
ENST00000642726.1:c.-64del	ENSP00000494353.1:n.-64del
ENST00000643296.1:c.-67del	ENSP00000496635.1:n.-67del
ENST00000643549.1:c.-64del	ENSP00000493975.1:n.-64del
ENST00000644737.1:c.-64del	ENSP00000495548.1:n.-64del
ENST00000644760.1:c.-140del	ENSP00000496682.1:n.-140del
ENST00000645460.1:c.-64del	ENSP00000494463.1:n.-64del
ENST00000646484.1:c.-64del	ENSP00000495536.1:n.-64del
ENST00000646510.1:c.-143del	ENSP00000494772.1:n.-143del
ENST00000646693.1:c.-64del	ENSP00000495368.1:n.-64del
ENST00000647230.1:c.-67del	ENSP00000494676.1:n.-67del
ENST00000344626.8:c.-67del	ENSP00000343896.4:n.-67del
ENST00000429416.7:c.-143del	ENSP00000395654.1:n.-143del
ENST00000444061.7:c.-67del	ENSP00000392837.2:n.-67del
ENST00000541122.6:c.-227del	ENSP00000445036.2:n.-227del
ENST00000589677.5:c.-296del	ENSP00000464778.1:n.-296del
NM_001128844.1:c.-143del	NP_001122316.1:n.-143del
NM_001128849.1:c.-67del	NP_001122321.1:n.-67del
NM_003072.3:c.-67del	NP_003063.2:n.-67del
XM_005260028.2:c.-67del	XP_005260085.1:n.-67del
XM_005260030.2:c.-67del	XP_005260087.1:n.-67del
XM_005260031.2:c.-67del	XP_005260088.1:n.-67del
XM_005260032.2:c.-67del	XP_005260089.1:n.-67del
XM_005260033.2:c.-67del	XP_005260090.1:n.-67del
XM_005260034.2:c.-67del	XP_005260091.1:n.-67del
XM_005260035.2:c.-67del	XP_005260092.1:n.-67del
XM_006722845.2:c.-64del	XP_006722908.1:n.-64del
XM_006722847.2:c.-67del	XP_006722910.1:n.-67del
XM_011528198.1:c.-143del	XP_011526500.1:n.-143del
XM_024451658.1:c.-140del	XP_024307426.1:n.-140del
XM_024451659.1:c.-67del	XP_024307427.1:n.-67del
XM_024451660.1:c.-67del	XP_024307428.1:n.-67del
XM_024451661.1:c.-67del	XP_024307429.1:n.-67del
XM_024451662.1:c.-67del	XP_024307430.1:n.-67del
XM_024451663.1:c.-67del	XP_024307431.1:n.-67del
XM_024451664.1:c.-67del	XP_024307432.1:n.-67del
XM_024451665.1:c.-67del	XP_024307433.1:n.-67del
XM_024451666.1:c.-67del	XP_024307434.1:n.-67del
XM_024451667.1:c.-67del	XP_024307435.1:n.-67del
NM_001128844.3:c.-143del	NP_001122316.1:n.-143del
NM_001128847.4:c.-67del	NP_001122319.1:n.-67del
NM_001128849.3:c.-67del	NP_001122321.1:n.-67del
NM_001374457.1:c.-64del	NP_001361386.1:n.-64del
NM_003072.5:c.-67del MANE Select	NP_003063.2:n.-67del
NR_164683.1:n.110del
NM_001387283.1:c.-64del MANE Plus Clinical	NP_001374212.1:n.-64del