Canonical Allele Identifier: CA431171129

Gene: SMARCAL1

Linked Data

• MyVariant Identifiers: chr2:g.217342959A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.216478236A>C , CM000664.2:g.216478236A>C	GRCh38
NC_000002.11:g.217342959A>C , CM000664.1:g.217342959A>C	GRCh37
NC_000002.10:g.217051204A>C	NCBI36
NG_009771.1:g.70823A>C , LRG_108:g.70823A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425815.6:c.2562A>C	ENSP00000394410.2:p.Ala854=
ENST00000430374.6:c.2562A>C	ENSP00000405077.2:p.Ala854=
ENST00000444508.6:c.2562A>C	ENSP00000398969.2:p.Ala854=
ENST00000697899.1:c.2328A>C	ENSP00000513470.1:p.Ala776=
ENST00000697901.1:c.*1317A>C	ENSP00000513471.1:n.*1317A>C
ENST00000697903.1:c.*1049A>C	ENSP00000513472.1:n.*1049A>C
ENST00000697904.1:c.*1049A>C	ENSP00000513473.1:n.*1049A>C
ENST00000697905.1:c.*1049A>C	ENSP00000513474.1:n.*1049A>C
ENST00000697906.1:c.2328A>C	ENSP00000513475.1:p.Ala776=
ENST00000697907.1:c.*1420A>C	ENSP00000513476.1:n.*1420A>C
ENST00000697908.1:n.2256A>C
ENST00000697909.1:n.1454A>C
ENST00000697910.1:n.959A>C
ENST00000697911.1:n.868A>C
ENST00000357276.9:c.2562A>C MANE Select	ENSP00000349823.4:p.Ala854=
ENST00000357276.8:c.2562A>C	ENSP00000349823.4:p.Ala854=
ENST00000358207.9:c.2562A>C	ENSP00000350940.5:p.Ala854=
ENST00000392128.6:c.2088A>C	ENSP00000375974.2:p.Ala696=
NM_001127207.1:c.2562A>C	NP_001120679.1:p.Ala854=
NM_014140.3:c.2562A>C , LRG_108t1:c.2562A>C	NP_054859.2:p.Ala854=
XM_005246631.2:c.2562A>C	XP_005246688.1:p.Ala854=
XM_005246632.1:c.2562A>C	XP_005246689.1:p.Ala854=
XM_006712557.1:c.2496A>C	XP_006712620.1:p.Ala832=
XM_005246632.2:c.2562A>C	XP_005246689.1:p.Ala854=
XM_017004228.2:c.1650A>C	XP_016859717.1:p.Ala550=
NM_001127207.2:c.2562A>C	NP_001120679.1:p.Ala854=
NM_014140.4:c.2562A>C MANE Select	NP_054859.2:p.Ala854=