Canonical Allele Identifier: CA2754245410

Gene: SMARCAL1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.216414670G>T , CM000664.2:g.216414670G>T	GRCh38
NC_000002.11:g.217279393G>T , CM000664.1:g.217279393G>T	GRCh37
NC_000002.10:g.216987638G>T	NCBI36
NG_009771.1:g.7257G>T , LRG_108:g.7257G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425815.6:c.-35G>T	ENSP00000394410.2:n.-35G>T
ENST00000430374.6:c.-35G>T	ENSP00000405077.2:n.-35G>T
ENST00000444508.6:c.-35G>T	ENSP00000398969.2:n.-35G>T
ENST00000697898.1:n.327G>T
ENST00000697899.1:c.-35G>T	ENSP00000513470.1:n.-35G>T
ENST00000697900.1:n.242G>T
ENST00000697901.1:c.-35G>T	ENSP00000513471.1:n.-35G>T
ENST00000697902.1:n.198G>T
ENST00000697903.1:c.-35G>T	ENSP00000513472.1:n.-35G>T
ENST00000697904.1:c.-35G>T	ENSP00000513473.1:n.-35G>T
ENST00000697905.1:c.-35G>T	ENSP00000513474.1:n.-35G>T
ENST00000697906.1:c.-35G>T	ENSP00000513475.1:n.-35G>T
ENST00000697907.1:c.-35G>T	ENSP00000513476.1:n.-35G>T
ENST00000357276.9:c.-35G>T MANE Select	ENSP00000349823.4:n.-35G>T
ENST00000357276.8:c.-35G>T	ENSP00000349823.4:n.-35G>T
ENST00000358207.9:c.-35G>T	ENSP00000350940.5:n.-35G>T
ENST00000425815.5:c.-35G>T	ENSP00000394410.1:n.-35G>T
ENST00000430374.5:c.-35G>T	ENSP00000405077.1:n.-35G>T
ENST00000434435.1:c.-35G>T	ENSP00000402967.1:n.-35G>T
ENST00000444508.5:c.-35G>T	ENSP00000398969.1:n.-35G>T
NM_001127207.1:c.-35G>T	NP_001120679.1:n.-35G>T
NM_014140.3:c.-35G>T , LRG_108t1:c.-35G>T	NP_054859.2:n.-35G>T
XM_005246631.2:c.-35G>T	XP_005246688.1:n.-35G>T
XM_005246632.1:c.-35G>T	XP_005246689.1:n.-35G>T
XM_006712557.1:c.-35G>T	XP_006712620.1:n.-35G>T
XM_005246632.2:c.-35G>T	XP_005246689.1:n.-35G>T
XM_017004228.2:c.-951G>T	XP_016859717.1:n.-951G>T
NM_001127207.2:c.-35G>T	NP_001120679.1:n.-35G>T
NM_014140.4:c.-35G>T MANE Select	NP_054859.2:n.-35G>T