Canonical Allele Identifier: CA350505591

Gene: SMARCAL1

Linked Data

• MyVariant Identifiers: chr2:g.217347669A>T (hg19) ; chr2:g.216482946A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.216482946A>T , CM000664.2:g.216482946A>T	GRCh38
NC_000002.11:g.217347669A>T , CM000664.1:g.217347669A>T	GRCh37
NC_000002.10:g.217055914A>T	NCBI36
NG_009771.1:g.75533A>T , LRG_108:g.75533A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425815.6:c.2834A>T	ENSP00000394410.2:p.Asp945Val
ENST00000430374.6:c.2834A>T	ENSP00000405077.2:p.Asp945Val
ENST00000444508.6:c.2834A>T	ENSP00000398969.2:p.Asp945Val
ENST00000697899.1:c.2600A>T	ENSP00000513470.1:p.Asp867Val
ENST00000697901.1:c.*1589A>T	ENSP00000513471.1:n.*1589A>T
ENST00000697903.1:c.*1321A>T	ENSP00000513472.1:n.*1321A>T
ENST00000697904.1:c.*1321A>T	ENSP00000513473.1:n.*1321A>T
ENST00000697905.1:c.*1321A>T	ENSP00000513474.1:n.*1321A>T
ENST00000697906.1:c.2600A>T	ENSP00000513475.1:p.Asp867Val
ENST00000697907.1:c.*1692A>T	ENSP00000513476.1:n.*1692A>T
ENST00000697909.1:n.1726A>T
ENST00000697910.1:n.1231A>T
ENST00000357276.9:c.2834A>T MANE Select	ENSP00000349823.4:p.Asp945Val
ENST00000357276.8:c.2834A>T	ENSP00000349823.4:p.Asp945Val
ENST00000358207.9:c.2834A>T	ENSP00000350940.5:p.Asp945Val
ENST00000392128.6:c.2360A>T	ENSP00000375974.2:p.Asp787Val
NM_001127207.1:c.2834A>T	NP_001120679.1:p.Asp945Val
NM_014140.3:c.2834A>T , LRG_108t1:c.2834A>T	NP_054859.2:p.Asp945Val
XM_005246631.2:c.2834A>T	XP_005246688.1:p.Asp945Val
XM_005246632.1:c.2834A>T	XP_005246689.1:p.Asp945Val
XM_006712557.1:c.2768A>T	XP_006712620.1:p.Asp923Val
XM_005246632.2:c.2834A>T	XP_005246689.1:p.Asp945Val
XM_017004228.2:c.1922A>T	XP_016859717.1:p.Asp641Val
NM_001127207.2:c.2834A>T	NP_001120679.1:p.Asp945Val
NM_014140.4:c.2834A>T MANE Select	NP_054859.2:p.Asp945Val