Canonical Allele Identifier: CA1327832945

Gene: SMARCAL1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.216441833_216441834delinsAC , CM000664.2:g.216441833_216441834delinsAC	GRCh38
NC_000002.11:g.217306556_217306557delinsAC , CM000664.1:g.217306556_217306557delinsAC	GRCh37
NC_000002.10:g.217014801_217014802delinsAC	NCBI36
NG_009771.1:g.34420_34421delinsAC , LRG_108:g.34420_34421delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000425815.6:c.1710+3348_1710+3349delinsAC	ENSP00000394410.2:n.1710+3348_1710+3349delinsAC
ENST00000430374.6:c.1710+3348_1710+3349delinsAC	ENSP00000405077.2:n.1710+3348_1710+3349delinsAC
ENST00000444508.6:c.1710+3348_1710+3349delinsAC	ENSP00000398969.2:n.1710+3348_1710+3349delinsAC
ENST00000697898.1:n.2071+3348_2071+3349delinsAC
ENST00000697899.1:c.1476+3348_1476+3349delinsAC	ENSP00000513470.1:n.1476+3348_1476+3349delinsAC
ENST00000697901.1:c.*568+3348_*568+3349delinsAC	ENSP00000513471.1:n.*568+3348_*568+3349delinsAC
ENST00000697902.1:n.1942+3348_1942+3349delinsAC
ENST00000697903.1:c.*197+3348_*197+3349delinsAC	ENSP00000513472.1:n.*197+3348_*197+3349delinsAC
ENST00000697904.1:c.*197+3348_*197+3349delinsAC	ENSP00000513473.1:n.*197+3348_*197+3349delinsAC
ENST00000697905.1:c.*197+3348_*197+3349delinsAC	ENSP00000513474.1:n.*197+3348_*197+3349delinsAC
ENST00000697906.1:c.1476+3348_1476+3349delinsAC	ENSP00000513475.1:n.1476+3348_1476+3349delinsAC
ENST00000697907.1:c.*568+3348_*568+3349delinsAC	ENSP00000513476.1:n.*568+3348_*568+3349delinsAC
ENST00000697908.1:n.1507+3348_1507+3349delinsAC
ENST00000697909.1:n.602+3348_602+3349delinsAC
ENST00000357276.9:c.1710+3348_1710+3349delinsAC MANE Select	ENSP00000349823.4:n.1710+3348_1710+3349delinsAC
ENST00000357276.8:c.1710+3348_1710+3349delinsAC	ENSP00000349823.4:n.1710+3348_1710+3349delinsAC
ENST00000358207.9:c.1710+3348_1710+3349delinsAC	ENSP00000350940.5:n.1710+3348_1710+3349delinsAC
ENST00000392128.6:c.1237-5185_1237-5184delinsAC	ENSP00000375974.2:n.1237-5185_1237-5184delinsAC
ENST00000445153.1:c.383+3348_383+3349delinsAC
NM_001127207.1:c.1710+3348_1710+3349delinsAC	NP_001120679.1:n.1710+3348_1710+3349delinsAC
NM_014140.3:c.1710+3348_1710+3349delinsAC , LRG_108t1:c.1710+3348_1710+3349delinsAC	NP_054859.2:n.1710+3348_1710+3349delinsAC
XM_005246631.2:c.1710+3348_1710+3349delinsAC	XP_005246688.1:n.1710+3348_1710+3349delinsAC
XM_005246632.1:c.1710+3348_1710+3349delinsAC	XP_005246689.1:n.1710+3348_1710+3349delinsAC
XM_006712557.1:c.1645-5185_1645-5184delinsAC	XP_006712620.1:n.1645-5185_1645-5184delinsAC
XM_005246632.2:c.1710+3348_1710+3349delinsAC	XP_005246689.1:n.1710+3348_1710+3349delinsAC
XM_017004228.2:c.798+3348_798+3349delinsAC	XP_016859717.1:n.798+3348_798+3349delinsAC
NM_001127207.2:c.1710+3348_1710+3349delinsAC	NP_001120679.1:n.1710+3348_1710+3349delinsAC
NM_014140.4:c.1710+3348_1710+3349delinsAC MANE Select	NP_054859.2:n.1710+3348_1710+3349delinsAC