Canonical Allele Identifier: CA16604116
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 392886
ClinVar RCV Id: RCV000421318
dbSNP Id: rs1057524680

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216428638T>C , CM000664.2:g.216428638T>C GRCh38
NC_000002.11:g.217293361T>C , CM000664.1:g.217293361T>C GRCh37
NC_000002.10:g.217001606T>C NCBI36
NG_009771.1:g.21225T>C , LRG_108:g.21225T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000425815.6:c.1190T>C ENSP00000394410.2:p.Leu397Pro
ENST00000430374.6:c.1190T>C ENSP00000405077.2:p.Leu397Pro
ENST00000444508.6:c.1190T>C ENSP00000398969.2:p.Leu397Pro
ENST00000697898.1:n.1551T>C
ENST00000697899.1:c.956T>C ENSP00000513470.1:p.Leu319Pro
ENST00000697900.1:n.1466T>C
ENST00000697901.1:c.*48T>C ENSP00000513471.1:n.*48T>C
ENST00000697902.1:n.1422T>C
ENST00000697903.1:c.1190T>C ENSP00000513472.1:p.Leu397Pro
ENST00000697904.1:c.1190T>C ENSP00000513473.1:p.Leu397Pro
ENST00000697905.1:c.1190T>C ENSP00000513474.1:p.Leu397Pro
ENST00000697906.1:c.956T>C ENSP00000513475.1:p.Leu319Pro
ENST00000697907.1:c.*48T>C ENSP00000513476.1:n.*48T>C
ENST00000697908.1:n.987T>C
ENST00000357276.9:c.1190T>C MANE Select ENSP00000349823.4:p.Leu397Pro
ENST00000357276.8:c.1190T>C ENSP00000349823.4:p.Leu397Pro
ENST00000358207.9:c.1190T>C ENSP00000350940.5:p.Leu397Pro
ENST00000392128.6:c.782T>C ENSP00000375974.2:p.Leu261Pro
ENST00000412913.1:c.350T>C ENSP00000390248.1:p.Leu117Pro
ENST00000427645.5:c.836T>C ENSP00000392997.1:p.Leu279Pro
ENST00000479008.1:n.434T>C
NM_001127207.1:c.1190T>C NP_001120679.1:p.Leu397Pro
NM_014140.3:c.1190T>C , LRG_108t1:c.1190T>C NP_054859.2:p.Leu397Pro
XM_005246631.2:c.1190T>C XP_005246688.1:p.Leu397Pro
XM_005246632.1:c.1190T>C XP_005246689.1:p.Leu397Pro
XM_006712557.1:c.1190T>C XP_006712620.1:p.Leu397Pro
XM_005246632.2:c.1190T>C XP_005246689.1:p.Leu397Pro
XM_017004228.2:c.278T>C XP_016859717.1:p.Leu93Pro
NM_001127207.2:c.1190T>C NP_001120679.1:p.Leu397Pro
NM_014140.4:c.1190T>C MANE Select NP_054859.2:p.Leu397Pro