Canonical Allele Identifier: CA350503919

Gene: SMARCAL1

Linked Data

• MyVariant Identifiers: chr2:g.217340010A>C (hg19) ; chr2:g.216475287A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.216475287A>C , CM000664.2:g.216475287A>C	GRCh38
NC_000002.11:g.217340010A>C , CM000664.1:g.217340010A>C	GRCh37
NC_000002.10:g.217048255A>C	NCBI36
NG_009771.1:g.67874A>C , LRG_108:g.67874A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425815.6:c.2263A>C	ENSP00000394410.2:p.Ile755Leu
ENST00000430374.6:c.2263A>C	ENSP00000405077.2:p.Ile755Leu
ENST00000444508.6:c.2263A>C	ENSP00000398969.2:p.Ile755Leu
ENST00000697899.1:c.2029A>C	ENSP00000513470.1:p.Ile677Leu
ENST00000697901.1:c.*1018A>C	ENSP00000513471.1:n.*1018A>C
ENST00000697903.1:c.*750A>C	ENSP00000513472.1:n.*750A>C
ENST00000697904.1:c.*750A>C	ENSP00000513473.1:n.*750A>C
ENST00000697905.1:c.*750A>C	ENSP00000513474.1:n.*750A>C
ENST00000697906.1:c.2029A>C	ENSP00000513475.1:p.Ile677Leu
ENST00000697907.1:c.*1121A>C	ENSP00000513476.1:n.*1121A>C
ENST00000697908.1:n.1957A>C
ENST00000697909.1:n.1155A>C
ENST00000697910.1:n.660A>C
ENST00000697911.1:n.569A>C
ENST00000357276.9:c.2263A>C MANE Select	ENSP00000349823.4:p.Ile755Leu
ENST00000357276.8:c.2263A>C	ENSP00000349823.4:p.Ile755Leu
ENST00000358207.9:c.2263A>C	ENSP00000350940.5:p.Ile755Leu
ENST00000392128.6:c.1789A>C	ENSP00000375974.2:p.Ile597Leu
NM_001127207.1:c.2263A>C	NP_001120679.1:p.Ile755Leu
NM_014140.3:c.2263A>C , LRG_108t1:c.2263A>C	NP_054859.2:p.Ile755Leu
XM_005246631.2:c.2263A>C	XP_005246688.1:p.Ile755Leu
XM_005246632.1:c.2263A>C	XP_005246689.1:p.Ile755Leu
XM_006712557.1:c.2197A>C	XP_006712620.1:p.Ile733Leu
XM_005246632.2:c.2263A>C	XP_005246689.1:p.Ile755Leu
XM_017004228.2:c.1351A>C	XP_016859717.1:p.Ile451Leu
NM_001127207.2:c.2263A>C	NP_001120679.1:p.Ile755Leu
NM_014140.4:c.2263A>C MANE Select	NP_054859.2:p.Ile755Leu