Canonical Allele Identifier: CA1327821591

Gene: SMARCAL1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.216415562_216415570delinsTGGAGTCTC , CM000664.2:g.216415562_216415570delinsTGGAGTCTC	GRCh38
NC_000002.11:g.217280285_217280293delinsTGGAGTCTC , CM000664.1:g.217280285_217280293delinsTGGAGTCTC	GRCh37
NC_000002.10:g.216988530_216988538delinsTGGAGTCTC	NCBI36
NG_009771.1:g.8149_8157delinsTGGAGTCTC , LRG_108:g.8149_8157delinsTGGAGTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425815.6:c.811+47_811+55delinsTGGAGTCTC	ENSP00000394410.2:n.811+47_811+55delinsTGGAGTCTC
ENST00000430374.6:c.811+47_811+55delinsTGGAGTCTC	ENSP00000405077.2:n.811+47_811+55delinsTGGAGTCTC
ENST00000444508.6:c.811+47_811+55delinsTGGAGTCTC	ENSP00000398969.2:n.811+47_811+55delinsTGGAGTCTC
ENST00000697898.1:n.1172+47_1172+55delinsTGGAGTCTC
ENST00000697899.1:c.811+47_811+55delinsTGGAGTCTC	ENSP00000513470.1:n.811+47_811+55delinsTGGAGTCTC
ENST00000697900.1:n.1087+47_1087+55delinsTGGAGTCTC
ENST00000697901.1:c.811+47_811+55delinsTGGAGTCTC	ENSP00000513471.1:n.811+47_811+55delinsTGGAGTCTC
ENST00000697902.1:n.1043+47_1043+55delinsTGGAGTCTC
ENST00000697903.1:c.811+47_811+55delinsTGGAGTCTC	ENSP00000513472.1:n.811+47_811+55delinsTGGAGTCTC
ENST00000697904.1:c.811+47_811+55delinsTGGAGTCTC	ENSP00000513473.1:n.811+47_811+55delinsTGGAGTCTC
ENST00000697905.1:c.811+47_811+55delinsTGGAGTCTC	ENSP00000513474.1:n.811+47_811+55delinsTGGAGTCTC
ENST00000697906.1:c.811+47_811+55delinsTGGAGTCTC	ENSP00000513475.1:n.811+47_811+55delinsTGGAGTCTC
ENST00000697907.1:c.811+47_811+55delinsTGGAGTCTC	ENSP00000513476.1:n.811+47_811+55delinsTGGAGTCTC
ENST00000357276.9:c.811+47_811+55delinsTGGAGTCTC MANE Select	ENSP00000349823.4:n.811+47_811+55delinsTGGAGTCTC
ENST00000357276.8:c.811+47_811+55delinsTGGAGTCTC	ENSP00000349823.4:n.811+47_811+55delinsTGGAGTCTC
ENST00000358207.9:c.811+47_811+55delinsTGGAGTCTC	ENSP00000350940.5:n.811+47_811+55delinsTGGAGTCTC
ENST00000392128.6:c.403+47_403+55delinsTGGAGTCTC	ENSP00000375974.2:n.403+47_403+55delinsTGGAGTCTC
ENST00000427645.5:c.508+47_508+55delinsTGGAGTCTC	ENSP00000392997.1:n.508+47_508+55delinsTGGAGTCTC
NM_001127207.1:c.811+47_811+55delinsTGGAGTCTC	NP_001120679.1:n.811+47_811+55delinsTGGAGTCTC
NM_014140.3:c.811+47_811+55delinsTGGAGTCTC , LRG_108t1:c.811+47_811+55delinsTGGAGTCTC	NP_054859.2:n.811+47_811+55delinsTGGAGTCTC
XM_005246631.2:c.811+47_811+55delinsTGGAGTCTC	XP_005246688.1:n.811+47_811+55delinsTGGAGTCTC
XM_005246632.1:c.811+47_811+55delinsTGGAGTCTC	XP_005246689.1:n.811+47_811+55delinsTGGAGTCTC
XM_006712557.1:c.811+47_811+55delinsTGGAGTCTC	XP_006712620.1:n.811+47_811+55delinsTGGAGTCTC
XM_005246632.2:c.811+47_811+55delinsTGGAGTCTC	XP_005246689.1:n.811+47_811+55delinsTGGAGTCTC
XM_017004228.2:c.-106+47_-106+55delinsTGGAGTCTC	XP_016859717.1:n.-106+47_-106+55delinsTGGAGTCTC
NM_001127207.2:c.811+47_811+55delinsTGGAGTCTC	NP_001120679.1:n.811+47_811+55delinsTGGAGTCTC
NM_014140.4:c.811+47_811+55delinsTGGAGTCTC MANE Select	NP_054859.2:n.811+47_811+55delinsTGGAGTCTC