Canonical Allele Identifier: CA1327851095

Gene: SMARCAL1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.216483037T= , CM000664.2:g.216483037T=	GRCh38
NC_000002.11:g.217347760T= , CM000664.1:g.217347760T=	GRCh37
NC_000002.10:g.217056005T=	NCBI36
NG_009771.1:g.75624T= , LRG_108:g.75624T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000430374.6:c.*60T=	ENSP00000405077.2:n.*60T=
ENST00000697899.1:c.*60T=	ENSP00000513470.1:n.*60T=
ENST00000357276.9:c.*60T= MANE Select	ENSP00000349823.4:n.*60T=
ENST00000357276.8:c.*60T=	ENSP00000349823.4:n.*60T=
NM_001127207.1:c.*60T=	NP_001120679.1:n.*60T=
NM_014140.3:c.*60T= , LRG_108t1:c.*60T=	NP_054859.2:n.*60T=
XM_005246631.2:c.*60T=	XP_005246688.1:n.*60T=
XM_005246632.1:c.*60T=	XP_005246689.1:n.*60T=
XM_006712557.1:c.*60T=	XP_006712620.1:n.*60T=
XM_005246632.2:c.*60T=	XP_005246689.1:n.*60T=
XM_017004228.2:c.*60T=	XP_016859717.1:n.*60T=
NM_001127207.2:c.*60T=	NP_001120679.1:n.*60T=
NM_014140.4:c.*60T= MANE Select	NP_054859.2:n.*60T=