Canonical Allele Identifier: CA431165571

Gene: SMARCAL1

Linked Data

• gnomAD v4: 2-216412623-G-T
• MyVariant Identifiers: chr2:g.217277346G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.216412623G>T , CM000664.2:g.216412623G>T	GRCh38
NC_000002.11:g.217277346G>T , CM000664.1:g.217277346G>T	GRCh37
NC_000002.10:g.216985591G>T	NCBI36
NG_009771.1:g.5210G>T , LRG_108:g.5210G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425815.6:c.-190G>T	ENSP00000394410.2:n.-190G>T
ENST00000430374.6:c.-96+20G>T	ENSP00000405077.2:n.-96+20G>T
ENST00000444508.6:c.-207G>T	ENSP00000398969.2:n.-207G>T
ENST00000697898.1:n.241G>T
ENST00000697899.1:c.-121G>T	ENSP00000513470.1:n.-121G>T
ENST00000697900.1:n.156G>T
ENST00000697901.1:c.-121G>T	ENSP00000513471.1:n.-121G>T
ENST00000697902.1:n.112G>T
ENST00000697903.1:c.-121G>T	ENSP00000513472.1:n.-121G>T
ENST00000357276.9:c.-121G>T MANE Select	ENSP00000349823.4:n.-121G>T
ENST00000357276.8:c.-121G>T	ENSP00000349823.4:n.-121G>T
ENST00000425815.5:c.-190G>T	ENSP00000394410.1:n.-190G>T
ENST00000430374.5:c.-96+20G>T	ENSP00000405077.1:n.-96+20G>T
ENST00000444508.5:c.-207G>T	ENSP00000398969.1:n.-207G>T
NM_014140.3:c.-121G>T , LRG_108t1:c.-121G>T	NP_054859.2:n.-121G>T
XM_005246631.2:c.-96+20G>T	XP_005246688.1:n.-96+20G>T
XM_005246632.1:c.-207G>T	XP_005246689.1:n.-207G>T
XM_006712557.1:c.-121G>T	XP_006712620.1:n.-121G>T
XM_005246632.2:c.-207G>T	XP_005246689.1:n.-207G>T
NM_014140.4:c.-121G>T MANE Select	NP_054859.2:n.-121G>T