Canonical Allele Identifier: CA350505457

Gene: SMARCAL1

Linked Data

• MyVariant Identifiers: chr2:g.217347612T>G (hg19) ; chr2:g.216482889T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.216482889T>G , CM000664.2:g.216482889T>G	GRCh38
NC_000002.11:g.217347612T>G , CM000664.1:g.217347612T>G	GRCh37
NC_000002.10:g.217055857T>G	NCBI36
NG_009771.1:g.75476T>G , LRG_108:g.75476T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425815.6:c.2777T>G	ENSP00000394410.2:p.Leu926Arg
ENST00000430374.6:c.2777T>G	ENSP00000405077.2:p.Leu926Arg
ENST00000444508.6:c.2777T>G	ENSP00000398969.2:p.Leu926Arg
ENST00000697899.1:c.2543T>G	ENSP00000513470.1:p.Leu848Arg
ENST00000697901.1:c.*1532T>G	ENSP00000513471.1:n.*1532T>G
ENST00000697903.1:c.*1264T>G	ENSP00000513472.1:n.*1264T>G
ENST00000697904.1:c.*1264T>G	ENSP00000513473.1:n.*1264T>G
ENST00000697905.1:c.*1264T>G	ENSP00000513474.1:n.*1264T>G
ENST00000697906.1:c.2543T>G	ENSP00000513475.1:p.Leu848Arg
ENST00000697907.1:c.*1635T>G	ENSP00000513476.1:n.*1635T>G
ENST00000697909.1:n.1669T>G
ENST00000697910.1:n.1174T>G
ENST00000357276.9:c.2777T>G MANE Select	ENSP00000349823.4:p.Leu926Arg
ENST00000357276.8:c.2777T>G	ENSP00000349823.4:p.Leu926Arg
ENST00000358207.9:c.2777T>G	ENSP00000350940.5:p.Leu926Arg
ENST00000392128.6:c.2303T>G	ENSP00000375974.2:p.Leu768Arg
NM_001127207.1:c.2777T>G	NP_001120679.1:p.Leu926Arg
NM_014140.3:c.2777T>G , LRG_108t1:c.2777T>G	NP_054859.2:p.Leu926Arg
XM_005246631.2:c.2777T>G	XP_005246688.1:p.Leu926Arg
XM_005246632.1:c.2777T>G	XP_005246689.1:p.Leu926Arg
XM_006712557.1:c.2711T>G	XP_006712620.1:p.Leu904Arg
XM_005246632.2:c.2777T>G	XP_005246689.1:p.Leu926Arg
XM_017004228.2:c.1865T>G	XP_016859717.1:p.Leu622Arg
NM_001127207.2:c.2777T>G	NP_001120679.1:p.Leu926Arg
NM_014140.4:c.2777T>G MANE Select	NP_054859.2:p.Leu926Arg