Canonical Allele Identifier: CA2495873284

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47476580_47476592delinsATCTCCTAGTCCC , CM000664.2:g.47476580_47476592delinsATCTCCTAGTCCC	GRCh38
NC_000002.11:g.47703719_47703731delinsATCTCCTAGTCCC , CM000664.1:g.47703719_47703731delinsATCTCCTAGTCCC	GRCh37
NC_000002.10:g.47557223_47557235delinsATCTCCTAGTCCC	NCBI36
NG_007110.2:g.78457_78469delinsATCTCCTAGTCCC , LRG_218:g.78457_78469delinsATCTCCTAGTCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2210+9_2210+21delinsATCTCCTAGTCCC	ENSP00000495641.2:n.2210+9_2210+21delinsATCTCCTAGTCCC
ENST00000233146.7:c.2210+9_2210+21delinsATCTCCTAGTCCC MANE Select	ENSP00000233146.2:n.2210+9_2210+21delinsATCTCCTAGTCCC
ENST00000543555.6:c.2012+9_2012+21delinsATCTCCTAGTCCC	ENSP00000442697.1:n.2012+9_2012+21delinsATCTCCTAGTCCC
ENST00000644092.1:c.*510+9_*510+21delinsATCTCCTAGTCCC	ENSP00000496351.1:n.*510+9_*510+21delinsATCTCCTAGTCCC
ENST00000644900.1:c.63+9_63+21delinsATCTCCTAGTCCC
ENST00000645339.1:c.2210+9_2210+21delinsATCTCCTAGTCCC	ENSP00000496441.1:n.2210+9_2210+21delinsATCTCCTAGTCCC
ENST00000645506.1:c.2210+9_2210+21delinsATCTCCTAGTCCC	ENSP00000495455.1:n.2210+9_2210+21delinsATCTCCTAGTCCC
ENST00000646415.1:c.2210+9_2210+21delinsATCTCCTAGTCCC	ENSP00000495543.1:n.2210+9_2210+21delinsATCTCCTAGTCCC
ENST00000233146.6:c.2210+9_2210+21delinsATCTCCTAGTCCC	ENSP00000233146.2:n.2210+9_2210+21delinsATCTCCTAGTCCC
ENST00000406134.5:c.2210+9_2210+21delinsATCTCCTAGTCCC	ENSP00000384199.1:n.2210+9_2210+21delinsATCTCCTAGTCCC
ENST00000543555.5:c.2012+9_2012+21delinsATCTCCTAGTCCC	ENSP00000442697.1:n.2012+9_2012+21delinsATCTCCTAGTCCC
ENST00000610696.4:c.*606+9_*606+21delinsATCTCCTAGTCCC	ENSP00000483159.1:n.*606+9_*606+21delinsATCTCCTAGTCCC
ENST00000613514.4:c.*750+9_*750+21delinsATCTCCTAGTCCC	ENSP00000484137.1:n.*750+9_*750+21delinsATCTCCTAGTCCC
ENST00000617333.3:c.*976+9_*976+21delinsATCTCCTAGTCCC	ENSP00000482468.1:n.*976+9_*976+21delinsATCTCCTAGTCCC
ENST00000617938.4:c.*1182+9_*1182+21delinsATCTCCTAGTCCC	ENSP00000481158.1:n.*1182+9_*1182+21delinsATCTCCTAGTCCC
ENST00000621359.2:c.2210+9_2210+21delinsATCTCCTAGTCCC	ENSP00000481416.1:n.2210+9_2210+21delinsATCTCCTAGTCCC
NM_000251.2:c.2210+9_2210+21delinsATCTCCTAGTCCC , LRG_218t1:c.2210+9_2210+21delinsATCTCCTAGTCCC	NP_000242.1:n.2210+9_2210+21delinsATCTCCTAGTCCC
NM_001258281.1:c.2012+9_2012+21delinsATCTCCTAGTCCC	NP_001245210.1:n.2012+9_2012+21delinsATCTCCTAGTCCC
XM_005264332.2:c.2210+9_2210+21delinsATCTCCTAGTCCC	XP_005264389.2:n.2210+9_2210+21delinsATCTCCTAGTCCC
XM_011532867.1:c.2210+9_2210+21delinsATCTCCTAGTCCC	XP_011531169.1:n.2210+9_2210+21delinsATCTCCTAGTCCC
XR_939685.1:n.2282+9_2282+21delinsATCTCCTAGTCCC
XM_005264332.4:c.2210+9_2210+21delinsATCTCCTAGTCCC	XP_005264389.2:n.2210+9_2210+21delinsATCTCCTAGTCCC
XM_011532867.2:c.2210+9_2210+21delinsATCTCCTAGTCCC	XP_011531169.1:n.2210+9_2210+21delinsATCTCCTAGTCCC
XR_001738747.2:n.2272+9_2272+21delinsATCTCCTAGTCCC
XR_939685.2:n.2272+9_2272+21delinsATCTCCTAGTCCC
NM_000251.3:c.2210+9_2210+21delinsATCTCCTAGTCCC MANE Select	NP_000242.1:n.2210+9_2210+21delinsATCTCCTAGTCCC