Canonical Allele Identifier: CA350499500

Gene: SMARCAL1

Linked Data

• gnomAD v4: 2-216428646-A-T
• MyVariant Identifiers: chr2:g.217293369A>T (hg19) ; chr2:g.216428646A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.216428646A>T , CM000664.2:g.216428646A>T	GRCh38
NC_000002.11:g.217293369A>T , CM000664.1:g.217293369A>T	GRCh37
NC_000002.10:g.217001614A>T	NCBI36
NG_009771.1:g.21233A>T , LRG_108:g.21233A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000425815.6:c.1198A>T	ENSP00000394410.2:p.Thr400Ser
ENST00000430374.6:c.1198A>T	ENSP00000405077.2:p.Thr400Ser
ENST00000444508.6:c.1198A>T	ENSP00000398969.2:p.Thr400Ser
ENST00000697898.1:n.1559A>T
ENST00000697899.1:c.964A>T	ENSP00000513470.1:p.Thr322Ser
ENST00000697900.1:n.1474A>T
ENST00000697901.1:c.*56A>T	ENSP00000513471.1:n.*56A>T
ENST00000697902.1:n.1430A>T
ENST00000697903.1:c.1198A>T	ENSP00000513472.1:p.Thr400Ser
ENST00000697904.1:c.1198A>T	ENSP00000513473.1:p.Thr400Ser
ENST00000697905.1:c.1198A>T	ENSP00000513474.1:p.Thr400Ser
ENST00000697906.1:c.964A>T	ENSP00000513475.1:p.Thr322Ser
ENST00000697907.1:c.*56A>T	ENSP00000513476.1:n.*56A>T
ENST00000697908.1:n.995A>T
ENST00000357276.9:c.1198A>T MANE Select	ENSP00000349823.4:p.Thr400Ser
ENST00000357276.8:c.1198A>T	ENSP00000349823.4:p.Thr400Ser
ENST00000358207.9:c.1198A>T	ENSP00000350940.5:p.Thr400Ser
ENST00000392128.6:c.790A>T	ENSP00000375974.2:p.Thr264Ser
ENST00000412913.1:c.358A>T	ENSP00000390248.1:p.Thr120Ser
ENST00000427645.5:c.844A>T	ENSP00000392997.1:p.Thr282Ser
ENST00000479008.1:n.442A>T
NM_001127207.1:c.1198A>T	NP_001120679.1:p.Thr400Ser
NM_014140.3:c.1198A>T , LRG_108t1:c.1198A>T	NP_054859.2:p.Thr400Ser
XM_005246631.2:c.1198A>T	XP_005246688.1:p.Thr400Ser
XM_005246632.1:c.1198A>T	XP_005246689.1:p.Thr400Ser
XM_006712557.1:c.1198A>T	XP_006712620.1:p.Thr400Ser
XM_005246632.2:c.1198A>T	XP_005246689.1:p.Thr400Ser
XM_017004228.2:c.286A>T	XP_016859717.1:p.Thr96Ser
NM_001127207.2:c.1198A>T	NP_001120679.1:p.Thr400Ser
NM_014140.4:c.1198A>T MANE Select	NP_054859.2:p.Thr400Ser