Canonical Allele Identifier: CA1327827150

Gene: SMARCAL1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.216428601A= , CM000664.2:g.216428601A=	GRCh38
NC_000002.11:g.217293324A= , CM000664.1:g.217293324A=	GRCh37
NC_000002.10:g.217001569A=	NCBI36
NG_009771.1:g.21188A= , LRG_108:g.21188A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425815.6:c.1153A=	ENSP00000394410.2:p.Lys385=
ENST00000430374.6:c.1153A=	ENSP00000405077.2:p.Lys385=
ENST00000444508.6:c.1153A=	ENSP00000398969.2:p.Lys385=
ENST00000697898.1:n.1514A=
ENST00000697899.1:c.919A=	ENSP00000513470.1:p.Lys307=
ENST00000697900.1:n.1429A=
ENST00000697901.1:c.*11A=	ENSP00000513471.1:n.*11A=
ENST00000697902.1:n.1385A=
ENST00000697903.1:c.1153A=	ENSP00000513472.1:p.Lys385=
ENST00000697904.1:c.1153A=	ENSP00000513473.1:p.Lys385=
ENST00000697905.1:c.1153A=	ENSP00000513474.1:p.Lys385=
ENST00000697906.1:c.919A=	ENSP00000513475.1:p.Lys307=
ENST00000697907.1:c.*11A=	ENSP00000513476.1:n.*11A=
ENST00000697908.1:n.950A=
ENST00000357276.9:c.1153A= MANE Select	ENSP00000349823.4:p.Lys385=
ENST00000357276.8:c.1153A=	ENSP00000349823.4:p.Lys385=
ENST00000358207.9:c.1153A=	ENSP00000350940.5:p.Lys385=
ENST00000392128.6:c.745A=	ENSP00000375974.2:p.Lys249=
ENST00000412913.1:c.313A=	ENSP00000390248.1:p.Lys105=
ENST00000427645.5:c.799A=	ENSP00000392997.1:p.Lys267=
ENST00000479008.1:n.397A=
NM_001127207.1:c.1153A=	NP_001120679.1:p.Lys385=
NM_014140.3:c.1153A= , LRG_108t1:c.1153A=	NP_054859.2:p.Lys385=
XM_005246631.2:c.1153A=	XP_005246688.1:p.Lys385=
XM_005246632.1:c.1153A=	XP_005246689.1:p.Lys385=
XM_006712557.1:c.1153A=	XP_006712620.1:p.Lys385=
XM_005246632.2:c.1153A=	XP_005246689.1:p.Lys385=
XM_017004228.2:c.241A=	XP_016859717.1:p.Lys81=
NM_001127207.2:c.1153A=	NP_001120679.1:p.Lys385=
NM_014140.4:c.1153A= MANE Select	NP_054859.2:p.Lys385=