Canonical Allele Identifier: CA1327849203

Gene: SMARCAL1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.216478259_216478260delinsAT , CM000664.2:g.216478259_216478260delinsAT	GRCh38
NC_000002.11:g.217342982_217342983delinsAT , CM000664.1:g.217342982_217342983delinsAT	GRCh37
NC_000002.10:g.217051227_217051228delinsAT	NCBI36
NG_009771.1:g.70846_70847delinsAT , LRG_108:g.70846_70847delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425815.6:c.2585_2586delinsAT	ENSP00000394410.2:p.Asn862=
ENST00000430374.6:c.2585_2586delinsAT	ENSP00000405077.2:p.Asn862=
ENST00000444508.6:c.2585_2586delinsAT	ENSP00000398969.2:p.Asn862=
ENST00000697899.1:c.2351_2352delinsAT	ENSP00000513470.1:p.Asn784=
ENST00000697901.1:c.*1340_*1341delinsAT	ENSP00000513471.1:n.*1340_*1341delinsAT
ENST00000697903.1:c.*1072_*1073delinsAT	ENSP00000513472.1:n.*1072_*1073delinsAT
ENST00000697904.1:c.*1072_*1073delinsAT	ENSP00000513473.1:n.*1072_*1073delinsAT
ENST00000697905.1:c.*1072_*1073delinsAT	ENSP00000513474.1:n.*1072_*1073delinsAT
ENST00000697906.1:c.2351_2352delinsAT	ENSP00000513475.1:p.Asn784=
ENST00000697907.1:c.*1443_*1444delinsAT	ENSP00000513476.1:n.*1443_*1444delinsAT
ENST00000697908.1:n.2279_2280delinsAT
ENST00000697909.1:n.1477_1478delinsAT
ENST00000697910.1:n.982_983delinsAT
ENST00000697911.1:n.891_892delinsAT
ENST00000357276.9:c.2585_2586delinsAT MANE Select	ENSP00000349823.4:p.Asn862=
ENST00000357276.8:c.2585_2586delinsAT	ENSP00000349823.4:p.Asn862=
ENST00000358207.9:c.2585_2586delinsAT	ENSP00000350940.5:p.Asn862=
ENST00000392128.6:c.2111_2112delinsAT	ENSP00000375974.2:p.Asn704=
NM_001127207.1:c.2585_2586delinsAT	NP_001120679.1:p.Asn862=
NM_014140.3:c.2585_2586delinsAT , LRG_108t1:c.2585_2586delinsAT	NP_054859.2:p.Asn862=
XM_005246631.2:c.2585_2586delinsAT	XP_005246688.1:p.Asn862=
XM_005246632.1:c.2585_2586delinsAT	XP_005246689.1:p.Asn862=
XM_006712557.1:c.2519_2520delinsAT	XP_006712620.1:p.Asn840=
XM_005246632.2:c.2585_2586delinsAT	XP_005246689.1:p.Asn862=
XM_017004228.2:c.1673_1674delinsAT	XP_016859717.1:p.Asn558=
NM_001127207.2:c.2585_2586delinsAT	NP_001120679.1:p.Asn862=
NM_014140.4:c.2585_2586delinsAT MANE Select	NP_054859.2:p.Asn862=