Canonical Allele Identifier: CA431164442

Gene: SMARCAL1

Linked Data

• MyVariant Identifiers: chr2:g.217277238T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.216412515T>G , CM000664.2:g.216412515T>G	GRCh38
NC_000002.11:g.217277238T>G , CM000664.1:g.217277238T>G	GRCh37
NC_000002.10:g.216985483T>G	NCBI36
NG_009771.1:g.5102T>G , LRG_108:g.5102T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000430374.6:c.-184T>G	ENSP00000405077.2:n.-184T>G
ENST00000444508.6:c.-315T>G	ENSP00000398969.2:n.-315T>G
ENST00000697898.1:n.133T>G
ENST00000697899.1:c.-229T>G	ENSP00000513470.1:n.-229T>G
ENST00000697900.1:n.48T>G
ENST00000697901.1:c.-229T>G	ENSP00000513471.1:n.-229T>G
ENST00000697902.1:n.4T>G
ENST00000697903.1:c.-229T>G	ENSP00000513472.1:n.-229T>G
ENST00000357276.9:c.-229T>G MANE Select	ENSP00000349823.4:n.-229T>G
ENST00000357276.8:c.-229T>G	ENSP00000349823.4:n.-229T>G
ENST00000430374.5:c.-184T>G	ENSP00000405077.1:n.-184T>G
ENST00000444508.5:c.-315T>G	ENSP00000398969.1:n.-315T>G
NM_014140.3:c.-229T>G , LRG_108t1:c.-229T>G	NP_054859.2:n.-229T>G
XM_005246631.2:c.-184T>G	XP_005246688.1:n.-184T>G
XM_005246632.1:c.-315T>G	XP_005246689.1:n.-315T>G
XM_006712557.1:c.-229T>G	XP_006712620.1:n.-229T>G
NM_014140.4:c.-229T>G MANE Select	NP_054859.2:n.-229T>G