Canonical Allele Identifier: CA505490418

Gene: SMARCA4

Linked Data

• MyVariant Identifiers: chr19:g.11134247G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11023571G>T , CM000681.2:g.11023571G>T	GRCh38
NC_000019.9:g.11134247G>T , CM000681.1:g.11134247G>T	GRCh37
NC_000019.8:g.10995247G>T	NCBI36
NG_011556.2:g.67650G>T
NG_011556.3:g.67640G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000711079.1:c.2913G>T	ENSP00000518564.1:p.Val971=
ENST00000704344.1:c.2913G>T	ENSP00000515855.1:p.Val971=
ENST00000704345.1:c.2904G>T	ENSP00000515856.1:p.Val968=
ENST00000646693.2:c.2913G>T MANE Plus Clinical	ENSP00000495368.1:p.Val971=
ENST00000344626.10:c.2913G>T MANE Select	ENSP00000343896.4:p.Val971=
ENST00000429416.8:c.2913G>T	ENSP00000395654.1:p.Val971=
ENST00000444061.8:c.2913G>T	ENSP00000392837.2:p.Val971=
ENST00000590574.6:c.2913G>T	ENSP00000466963.1:p.Val971=
ENST00000591545.6:c.2786G>T
ENST00000592604.6:n.1244G>T
ENST00000642350.1:c.1398G>T	ENSP00000495355.1:p.Val466=
ENST00000642508.1:c.274G>T
ENST00000642628.1:c.2913G>T	ENSP00000496498.1:p.Val971=
ENST00000642726.1:c.2913G>T	ENSP00000494353.1:p.Val971=
ENST00000643208.1:c.1470G>T	ENSP00000496074.1:p.Val490=
ENST00000643296.1:c.2913G>T	ENSP00000496635.1:p.Val971=
ENST00000643534.1:c.1198G>T
ENST00000643549.1:c.2913G>T	ENSP00000493975.1:p.Val971=
ENST00000643857.1:c.1268G>T
ENST00000643995.1:c.2327G>T
ENST00000644065.1:c.1640G>T
ENST00000644267.1:n.1268G>T
ENST00000644290.1:c.1170G>T
ENST00000644327.1:c.1684G>T
ENST00000644737.1:c.2913G>T	ENSP00000495548.1:p.Val971=
ENST00000644963.1:c.1558G>T
ENST00000645061.1:c.1401G>T	ENSP00000493690.1:p.Val467=
ENST00000645460.1:c.2913G>T	ENSP00000494463.1:p.Val971=
ENST00000645648.1:c.777G>T	ENSP00000493521.1:p.Val259=
ENST00000646183.1:c.1259G>T
ENST00000646236.1:c.396G>T	ENSP00000493925.1:p.Val132=
ENST00000646484.1:c.2913G>T	ENSP00000495536.1:p.Val971=
ENST00000646510.1:c.2913G>T	ENSP00000494772.1:p.Val971=
ENST00000646513.1:c.747G>T	ENSP00000495457.1:p.Val249=
ENST00000646593.1:c.761G>T	ENSP00000494341.1:n.761G>T
ENST00000646693.1:c.2913G>T	ENSP00000495368.1:p.Val971=
ENST00000646746.1:c.1213G>T
ENST00000647230.1:c.2913G>T	ENSP00000494676.1:p.Val971=
ENST00000647268.1:c.1266G>T	ENSP00000496176.1:p.Val422=
ENST00000344626.8:c.2913G>T	ENSP00000343896.4:p.Val971=
ENST00000413806.7:c.3105G>T	ENSP00000414727.3:p.Val1035=
ENST00000429416.7:c.2913G>T	ENSP00000395654.1:p.Val971=
ENST00000444061.7:c.2913G>T	ENSP00000392837.2:p.Val971=
ENST00000450717.7:c.2913G>T	ENSP00000397783.3:p.Val971=
ENST00000541122.6:c.2913G>T	ENSP00000445036.2:p.Val971=
ENST00000585799.5:n.1441G>T
ENST00000586122.5:n.495G>T
ENST00000589677.5:c.2913G>T	ENSP00000464778.1:p.Val971=
ENST00000590574.5:c.2913G>T	ENSP00000466963.1:p.Val971=
ENST00000591545.5:n.2787G>T
ENST00000591595.5:n.985G>T
ENST00000592604.5:n.826G>T
NM_001128844.1:c.2913G>T	NP_001122316.1:p.Val971=
NM_001128845.1:c.2913G>T	NP_001122317.1:p.Val971=
NM_001128846.1:c.2913G>T	NP_001122318.1:p.Val971=
NM_001128847.1:c.2913G>T	NP_001122319.1:p.Val971=
NM_001128848.1:c.2913G>T	NP_001122320.1:p.Val971=
NM_001128849.1:c.2913G>T	NP_001122321.1:p.Val971=
NM_003072.3:c.2913G>T	NP_003063.2:p.Val971=
XM_005260028.2:c.2913G>T	XP_005260085.1:p.Val971=
XM_005260030.2:c.2913G>T	XP_005260087.1:p.Val971=
XM_005260031.2:c.2913G>T	XP_005260088.1:p.Val971=
XM_005260032.2:c.2913G>T	XP_005260089.1:p.Val971=
XM_005260033.2:c.2913G>T	XP_005260090.1:p.Val971=
XM_005260034.2:c.2913G>T	XP_005260091.1:p.Val971=
XM_005260035.2:c.2913G>T	XP_005260092.1:p.Val971=
XM_006722845.2:c.2913G>T	XP_006722908.1:p.Val971=
XM_006722846.2:c.2913G>T	XP_006722909.1:p.Val971=
XM_006722847.2:c.2913G>T	XP_006722910.1:p.Val971=
XM_011528198.1:c.2913G>T	XP_011526500.1:p.Val971=
XM_024451658.1:c.2913G>T	XP_024307426.1:p.Val971=
XM_024451659.1:c.2913G>T	XP_024307427.1:p.Val971=
XM_024451660.1:c.2913G>T	XP_024307428.1:p.Val971=
XM_024451661.1:c.2913G>T	XP_024307429.1:p.Val971=
XM_024451662.1:c.2913G>T	XP_024307430.1:p.Val971=
XM_024451663.1:c.2913G>T	XP_024307431.1:p.Val971=
XM_024451664.1:c.2913G>T	XP_024307432.1:p.Val971=
XM_024451665.1:c.2913G>T	XP_024307433.1:p.Val971=
XM_024451666.1:c.2913G>T	XP_024307434.1:p.Val971=
XM_024451667.1:c.2913G>T	XP_024307435.1:p.Val971=
NM_001128844.3:c.2913G>T	NP_001122316.1:p.Val971=
NM_001128845.2:c.2913G>T	NP_001122317.1:p.Val971=
NM_001128846.2:c.2913G>T	NP_001122318.1:p.Val971=
NM_001128847.4:c.2913G>T	NP_001122319.1:p.Val971=
NM_001128848.2:c.2913G>T	NP_001122320.1:p.Val971=
NM_001128849.3:c.2913G>T	NP_001122321.1:p.Val971=
NM_001374457.1:c.2913G>T	NP_001361386.1:p.Val971=
NM_003072.5:c.2913G>T MANE Select	NP_003063.2:p.Val971=
NR_164683.1:n.3203G>T
NM_001387283.1:c.2913G>T MANE Plus Clinical	NP_001374212.1:p.Val971=