Canonical Allele Identifier: CA2663032618

Gene: SMARCAL1

Linked Data

• gnomAD v4: 2-216415500-CCCAGCAAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.216415501_216415508del , CM000664.2:g.216415501_216415508del	GRCh38
NC_000002.11:g.217280224_217280231del , CM000664.1:g.217280224_217280231del	GRCh37
NC_000002.10:g.216988469_216988476del	NCBI36
NG_009771.1:g.8088_8095del , LRG_108:g.8088_8095del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425815.6:c.797_804del	ENSP00000394410.2:p.Pro266GlnfsTer3
ENST00000430374.6:c.797_804del	ENSP00000405077.2:p.Pro266GlnfsTer3
ENST00000444508.6:c.797_804del	ENSP00000398969.2:p.Pro266GlnfsTer3
ENST00000697898.1:n.1158_1165del
ENST00000697899.1:c.797_804del	ENSP00000513470.1:p.Pro266GlnfsTer3
ENST00000697900.1:n.1073_1080del
ENST00000697901.1:c.797_804del	ENSP00000513471.1:p.Pro266GlnfsTer3
ENST00000697902.1:n.1029_1036del
ENST00000697903.1:c.797_804del	ENSP00000513472.1:p.Pro266GlnfsTer3
ENST00000697904.1:c.797_804del	ENSP00000513473.1:p.Pro266GlnfsTer3
ENST00000697905.1:c.797_804del	ENSP00000513474.1:p.Pro266GlnfsTer3
ENST00000697906.1:c.797_804del	ENSP00000513475.1:p.Pro266GlnfsTer3
ENST00000697907.1:c.797_804del	ENSP00000513476.1:p.Pro266GlnfsTer3
ENST00000357276.9:c.797_804del MANE Select	ENSP00000349823.4:p.Pro266GlnfsTer3
ENST00000357276.8:c.797_804del	ENSP00000349823.4:p.Pro266GlnfsTer3
ENST00000358207.9:c.797_804del	ENSP00000350940.5:p.Pro266GlnfsTer3
ENST00000392128.6:c.389_396del	ENSP00000375974.2:p.Pro130GlnfsTer3
ENST00000427645.5:c.494_501del	ENSP00000392997.1:p.Pro165GlnfsTer3
NM_001127207.1:c.797_804del	NP_001120679.1:p.Pro266GlnfsTer3
NM_014140.3:c.797_804del , LRG_108t1:c.797_804del	NP_054859.2:p.Pro266GlnfsTer3
XM_005246631.2:c.797_804del	XP_005246688.1:p.Pro266GlnfsTer3
XM_005246632.1:c.797_804del	XP_005246689.1:p.Pro266GlnfsTer3
XM_006712557.1:c.797_804del	XP_006712620.1:p.Pro266GlnfsTer3
XM_005246632.2:c.797_804del	XP_005246689.1:p.Pro266GlnfsTer3
XM_017004228.2:c.-120_-113del	XP_016859717.1:n.-120_-113del
NM_001127207.2:c.797_804del	NP_001120679.1:p.Pro266GlnfsTer3
NM_014140.4:c.797_804del MANE Select	NP_054859.2:p.Pro266GlnfsTer3