Canonical Allele Identifier: CA2582453061

Gene: SMARCA4

Linked Data

• gnomAD v4: 19-10961047-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10961047T>C , CM000681.2:g.10961047T>C	GRCh38
NC_000019.9:g.11071723T>C , CM000681.1:g.11071723T>C	GRCh37
NC_000019.8:g.10932723T>C	NCBI36
NG_011556.2:g.5126T>C
NG_011556.3:g.5116T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000711079.1:c.-159T>C	ENSP00000518564.1:n.-159T>C
ENST00000646693.2:c.-156T>C MANE Plus Clinical	ENSP00000495368.1:n.-156T>C
ENST00000344626.10:c.-159T>C MANE Select	ENSP00000343896.4:n.-159T>C
ENST00000429416.8:c.-235T>C	ENSP00000395654.1:n.-235T>C
ENST00000642628.1:c.-159T>C	ENSP00000496498.1:n.-159T>C
ENST00000642726.1:c.-156T>C	ENSP00000494353.1:n.-156T>C
ENST00000643296.1:c.-159T>C	ENSP00000496635.1:n.-159T>C
ENST00000643549.1:c.-156T>C	ENSP00000493975.1:n.-156T>C
ENST00000644737.1:c.-156T>C	ENSP00000495548.1:n.-156T>C
ENST00000644760.1:c.-232T>C	ENSP00000496682.1:n.-232T>C
ENST00000645460.1:c.-156T>C	ENSP00000494463.1:n.-156T>C
ENST00000646484.1:c.-156T>C	ENSP00000495536.1:n.-156T>C
ENST00000646510.1:c.-235T>C	ENSP00000494772.1:n.-235T>C
ENST00000646693.1:c.-156T>C	ENSP00000495368.1:n.-156T>C
ENST00000647230.1:c.-159T>C	ENSP00000494676.1:n.-159T>C
ENST00000344626.8:c.-159T>C	ENSP00000343896.4:n.-159T>C
ENST00000429416.7:c.-235T>C	ENSP00000395654.1:n.-235T>C
NM_001128844.1:c.-235T>C	NP_001122316.1:n.-235T>C
NM_003072.3:c.-159T>C	NP_003063.2:n.-159T>C
XM_005260028.2:c.-159T>C	XP_005260085.1:n.-159T>C
XM_005260030.2:c.-159T>C	XP_005260087.1:n.-159T>C
XM_005260031.2:c.-159T>C	XP_005260088.1:n.-159T>C
XM_005260032.2:c.-159T>C	XP_005260089.1:n.-159T>C
XM_005260033.2:c.-159T>C	XP_005260090.1:n.-159T>C
XM_005260034.2:c.-159T>C	XP_005260091.1:n.-159T>C
XM_005260035.2:c.-159T>C	XP_005260092.1:n.-159T>C
XM_006722845.2:c.-156T>C	XP_006722908.1:n.-156T>C
XM_006722847.2:c.-159T>C	XP_006722910.1:n.-159T>C
XM_011528198.1:c.-235T>C	XP_011526500.1:n.-235T>C
XM_024451659.1:c.-159T>C	XP_024307427.1:n.-159T>C
XM_024451660.1:c.-159T>C	XP_024307428.1:n.-159T>C
XM_024451661.1:c.-159T>C	XP_024307429.1:n.-159T>C
XM_024451662.1:c.-159T>C	XP_024307430.1:n.-159T>C
XM_024451663.1:c.-159T>C	XP_024307431.1:n.-159T>C
XM_024451664.1:c.-159T>C	XP_024307432.1:n.-159T>C
XM_024451665.1:c.-159T>C	XP_024307433.1:n.-159T>C
XM_024451666.1:c.-159T>C	XP_024307434.1:n.-159T>C
XM_024451667.1:c.-159T>C	XP_024307435.1:n.-159T>C
NM_001128844.3:c.-235T>C	NP_001122316.1:n.-235T>C
NM_001128847.4:c.-159T>C	NP_001122319.1:n.-159T>C
NM_001128849.3:c.-159T>C	NP_001122321.1:n.-159T>C
NM_001374457.1:c.-156T>C	NP_001361386.1:n.-156T>C
NM_003072.5:c.-159T>C MANE Select	NP_003063.2:n.-159T>C
NR_164683.1:n.18T>C
NM_001387283.1:c.-156T>C MANE Plus Clinical	NP_001374212.1:n.-156T>C