Canonical Allele Identifier: CA246129
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 197797
dbSNP Id: rs148752234

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216420398G>A , CM000664.2:g.216420398G>A GRCh38
NC_000002.11:g.217285121G>A , CM000664.1:g.217285121G>A GRCh37
NC_000002.10:g.216993366G>A NCBI36
NG_009771.1:g.12985G>A , LRG_108:g.12985G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000425815.6:c.962G>A ENSP00000394410.2:p.Gly321Asp
ENST00000430374.6:c.962G>A ENSP00000405077.2:p.Gly321Asp
ENST00000444508.6:c.962G>A ENSP00000398969.2:p.Gly321Asp
ENST00000697898.1:n.1323G>A
ENST00000697899.1:c.863-3235G>A ENSP00000513470.1:n.863-3235G>A
ENST00000697900.1:n.1238G>A
ENST00000697901.1:c.962G>A ENSP00000513471.1:p.Gly321Asp
ENST00000697902.1:n.1194G>A
ENST00000697903.1:c.962G>A ENSP00000513472.1:p.Gly321Asp
ENST00000697904.1:c.962G>A ENSP00000513473.1:p.Gly321Asp
ENST00000697905.1:c.962G>A ENSP00000513474.1:p.Gly321Asp
ENST00000697906.1:c.863-3235G>A ENSP00000513475.1:n.863-3235G>A
ENST00000697907.1:c.962G>A ENSP00000513476.1:p.Gly321Asp
ENST00000357276.9:c.962G>A MANE Select ENSP00000349823.4:p.Gly321Asp
ENST00000357276.8:c.962G>A ENSP00000349823.4:p.Gly321Asp
ENST00000358207.9:c.962G>A ENSP00000350940.5:p.Gly321Asp
ENST00000392128.6:c.554G>A ENSP00000375974.2:p.Gly185Asp
ENST00000412913.1:c.122G>A ENSP00000390248.1:p.Gly41Asp
ENST00000427645.5:c.659G>A ENSP00000392997.1:p.Gly220Asp
NM_001127207.1:c.962G>A NP_001120679.1:p.Gly321Asp
NM_014140.3:c.962G>A , LRG_108t1:c.962G>A NP_054859.2:p.Gly321Asp
XM_005246631.2:c.962G>A XP_005246688.1:p.Gly321Asp
XM_005246632.1:c.962G>A XP_005246689.1:p.Gly321Asp
XM_006712557.1:c.962G>A XP_006712620.1:p.Gly321Asp
XM_005246632.2:c.962G>A XP_005246689.1:p.Gly321Asp
XM_017004228.2:c.46G>A XP_016859717.1:p.Ala16Thr
NM_001127207.2:c.962G>A NP_001120679.1:p.Gly321Asp
NM_014140.4:c.962G>A MANE Select NP_054859.2:p.Gly321Asp