Canonical Allele Identifier: CA2577238874

Gene: SMARCAL1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.216477054del , CM000664.2:g.216477054del	GRCh38
NC_000002.11:g.217341777del , CM000664.1:g.217341777del	GRCh37
NC_000002.10:g.217050022del	NCBI36
NG_009771.1:g.69641del , LRG_108:g.69641del

Transcript Alleles

HGVS	Amino-acid change
ENST00000425815.6:c.2428-55del	ENSP00000394410.2:n.2428-55del
ENST00000430374.6:c.2428-55del	ENSP00000405077.2:n.2428-55del
ENST00000444508.6:c.2428-55del	ENSP00000398969.2:n.2428-55del
ENST00000697899.1:c.2194-55del	ENSP00000513470.1:n.2194-55del
ENST00000697901.1:c.*1183-55del	ENSP00000513471.1:n.*1183-55del
ENST00000697903.1:c.*915-55del	ENSP00000513472.1:n.*915-55del
ENST00000697904.1:c.*915-55del	ENSP00000513473.1:n.*915-55del
ENST00000697905.1:c.*915-55del	ENSP00000513474.1:n.*915-55del
ENST00000697906.1:c.2194-55del	ENSP00000513475.1:n.2194-55del
ENST00000697907.1:c.*1286-55del	ENSP00000513476.1:n.*1286-55del
ENST00000697908.1:n.2122-55del
ENST00000697909.1:n.1320-55del
ENST00000697910.1:n.825-55del
ENST00000697911.1:n.734-55del
ENST00000357276.9:c.2428-55del MANE Select	ENSP00000349823.4:n.2428-55del
ENST00000357276.8:c.2428-55del	ENSP00000349823.4:n.2428-55del
ENST00000358207.9:c.2428-55del	ENSP00000350940.5:n.2428-55del
ENST00000392128.6:c.1954-55del	ENSP00000375974.2:n.1954-55del
NM_001127207.1:c.2428-55del	NP_001120679.1:n.2428-55del
NM_014140.3:c.2428-55del , LRG_108t1:c.2428-55del	NP_054859.2:n.2428-55del
XM_005246631.2:c.2428-55del	XP_005246688.1:n.2428-55del
XM_005246632.1:c.2428-55del	XP_005246689.1:n.2428-55del
XM_006712557.1:c.2362-55del	XP_006712620.1:n.2362-55del
XM_005246632.2:c.2428-55del	XP_005246689.1:n.2428-55del
XM_017004228.2:c.1516-55del	XP_016859717.1:n.1516-55del
NM_001127207.2:c.2428-55del	NP_001120679.1:n.2428-55del
NM_014140.4:c.2428-55del MANE Select	NP_054859.2:n.2428-55del