Canonical Allele Identifier: CA350505066

Gene: SMARCAL1

Linked Data

• dbSNP Id: rs1695131114
• MyVariant Identifiers: chr2:g.217343006C>A (hg19) ; chr2:g.216478283C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.216478283C>A , CM000664.2:g.216478283C>A	GRCh38
NC_000002.11:g.217343006C>A , CM000664.1:g.217343006C>A	GRCh37
NC_000002.10:g.217051251C>A	NCBI36
NG_009771.1:g.70870C>A , LRG_108:g.70870C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425815.6:c.2609C>A	ENSP00000394410.2:p.Thr870Asn
ENST00000430374.6:c.2609C>A	ENSP00000405077.2:p.Thr870Asn
ENST00000444508.6:c.2609C>A	ENSP00000398969.2:p.Thr870Asn
ENST00000697899.1:c.2375C>A	ENSP00000513470.1:p.Thr792Asn
ENST00000697901.1:c.*1364C>A	ENSP00000513471.1:n.*1364C>A
ENST00000697903.1:c.*1096C>A	ENSP00000513472.1:n.*1096C>A
ENST00000697904.1:c.*1096C>A	ENSP00000513473.1:n.*1096C>A
ENST00000697905.1:c.*1096C>A	ENSP00000513474.1:n.*1096C>A
ENST00000697906.1:c.2375C>A	ENSP00000513475.1:p.Thr792Asn
ENST00000697907.1:c.*1467C>A	ENSP00000513476.1:n.*1467C>A
ENST00000697908.1:n.2303C>A
ENST00000697909.1:n.1501C>A
ENST00000697910.1:n.1006C>A
ENST00000697911.1:n.915C>A
ENST00000357276.9:c.2609C>A MANE Select	ENSP00000349823.4:p.Thr870Asn
ENST00000357276.8:c.2609C>A	ENSP00000349823.4:p.Thr870Asn
ENST00000358207.9:c.2609C>A	ENSP00000350940.5:p.Thr870Asn
ENST00000392128.6:c.2135C>A	ENSP00000375974.2:p.Thr712Asn
NM_001127207.1:c.2609C>A	NP_001120679.1:p.Thr870Asn
NM_014140.3:c.2609C>A , LRG_108t1:c.2609C>A	NP_054859.2:p.Thr870Asn
XM_005246631.2:c.2609C>A	XP_005246688.1:p.Thr870Asn
XM_005246632.1:c.2609C>A	XP_005246689.1:p.Thr870Asn
XM_006712557.1:c.2543C>A	XP_006712620.1:p.Thr848Asn
XM_005246632.2:c.2609C>A	XP_005246689.1:p.Thr870Asn
XM_017004228.2:c.1697C>A	XP_016859717.1:p.Thr566Asn
NM_001127207.2:c.2609C>A	NP_001120679.1:p.Thr870Asn
NM_014140.4:c.2609C>A MANE Select	NP_054859.2:p.Thr870Asn