Canonical Allele Identifier: CA350497138

Gene: SMARCAL1

Linked Data

• ClinVar Variation Id: 935546
• ClinVar RCV Id: RCV001204167
• dbSNP Id: rs1693557419
• MyVariant Identifiers: chr2:g.217279791A>G (hg19) ; chr2:g.216415068A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.216415068A>G , CM000664.2:g.216415068A>G	GRCh38
NC_000002.11:g.217279791A>G , CM000664.1:g.217279791A>G	GRCh37
NC_000002.10:g.216988036A>G	NCBI36
NG_009771.1:g.7655A>G , LRG_108:g.7655A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425815.6:c.364A>G	ENSP00000394410.2:p.Ile122Val
ENST00000430374.6:c.364A>G	ENSP00000405077.2:p.Ile122Val
ENST00000444508.6:c.364A>G	ENSP00000398969.2:p.Ile122Val
ENST00000697898.1:n.725A>G
ENST00000697899.1:c.364A>G	ENSP00000513470.1:p.Ile122Val
ENST00000697900.1:n.640A>G
ENST00000697901.1:c.364A>G	ENSP00000513471.1:p.Ile122Val
ENST00000697902.1:n.596A>G
ENST00000697903.1:c.364A>G	ENSP00000513472.1:p.Ile122Val
ENST00000697904.1:c.364A>G	ENSP00000513473.1:p.Ile122Val
ENST00000697905.1:c.364A>G	ENSP00000513474.1:p.Ile122Val
ENST00000697906.1:c.364A>G	ENSP00000513475.1:p.Ile122Val
ENST00000697907.1:c.364A>G	ENSP00000513476.1:p.Ile122Val
ENST00000357276.9:c.364A>G MANE Select	ENSP00000349823.4:p.Ile122Val
ENST00000357276.8:c.364A>G	ENSP00000349823.4:p.Ile122Val
ENST00000358207.9:c.364A>G	ENSP00000350940.5:p.Ile122Val
ENST00000427645.5:c.61A>G	ENSP00000392997.1:p.Ile21Val
ENST00000430374.5:c.364A>G	ENSP00000405077.1:p.Ile122Val
ENST00000444508.5:c.364A>G	ENSP00000398969.1:p.Ile122Val
NM_001127207.1:c.364A>G	NP_001120679.1:p.Ile122Val
NM_014140.3:c.364A>G , LRG_108t1:c.364A>G	NP_054859.2:p.Ile122Val
XM_005246631.2:c.364A>G	XP_005246688.1:p.Ile122Val
XM_005246632.1:c.364A>G	XP_005246689.1:p.Ile122Val
XM_006712557.1:c.364A>G	XP_006712620.1:p.Ile122Val
XM_005246632.2:c.364A>G	XP_005246689.1:p.Ile122Val
XM_017004228.2:c.-553A>G	XP_016859717.1:n.-553A>G
NM_001127207.2:c.364A>G	NP_001120679.1:p.Ile122Val
NM_014140.4:c.364A>G MANE Select	NP_054859.2:p.Ile122Val