Canonical Allele Identifier: CA2495877505

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47483140_47483144delinsGTAAC , CM000664.2:g.47483140_47483144delinsGTAAC	GRCh38
NC_000002.11:g.47710279_47710283delinsGTAAC , CM000664.1:g.47710279_47710283delinsGTAAC	GRCh37
NC_000002.10:g.47563783_47563787delinsGTAAC	NCBI36
NG_007110.2:g.85017_85021delinsGTAAC , LRG_218:g.85017_85021delinsGTAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2634+2269_2634+2273delinsGTAAC	ENSP00000495641.2:n.2634+2269_2634+2273delinsGTAAC
ENST00000233146.7:c.*191_*195delinsGTAAC MANE Select	ENSP00000233146.2:n.*191_*195delinsGTAAC
ENST00000543555.6:c.*191_*195delinsGTAAC	ENSP00000442697.1:n.*191_*195delinsGTAAC
ENST00000644092.1:c.*934+2269_*934+2273delinsGTAAC	ENSP00000496351.1:n.*934+2269_*934+2273delinsGTAAC
ENST00000644900.1:c.487+2269_487+2273delinsGTAAC
ENST00000645339.1:c.2634+2269_2634+2273delinsGTAAC	ENSP00000496441.1:n.2634+2269_2634+2273delinsGTAAC
ENST00000645506.1:c.2634+2269_2634+2273delinsGTAAC	ENSP00000495455.1:n.2634+2269_2634+2273delinsGTAAC
ENST00000646415.1:c.2634+2269_2634+2273delinsGTAAC	ENSP00000495543.1:n.2634+2269_2634+2273delinsGTAAC
ENST00000233146.6:c.*191_*195delinsGTAAC	ENSP00000233146.2:n.*191_*195delinsGTAAC
ENST00000406134.5:c.2634+2269_2634+2273delinsGTAAC	ENSP00000384199.1:n.2634+2269_2634+2273delinsGTAAC
ENST00000461394.5:n.75+2269_75+2273delinsGTAAC
ENST00000543555.5:c.*191_*195delinsGTAAC	ENSP00000442697.1:n.*191_*195delinsGTAAC
NM_000251.2:c.*191_*195delinsGTAAC , LRG_218t1:c.*191_*195delinsGTAAC	NP_000242.1:n.*191_*195delinsGTAAC
NM_001258281.1:c.*191_*195delinsGTAAC	NP_001245210.1:n.*191_*195delinsGTAAC
XM_005264332.2:c.2634+2269_2634+2273delinsGTAAC	XP_005264389.2:n.2634+2269_2634+2273delinsGTAAC
XM_011532867.1:c.2634+2269_2634+2273delinsGTAAC	XP_011531169.1:n.2634+2269_2634+2273delinsGTAAC
XR_939685.1:n.2706+2269_2706+2273delinsGTAAC
XM_005264332.4:c.2634+2269_2634+2273delinsGTAAC	XP_005264389.2:n.2634+2269_2634+2273delinsGTAAC
XM_011532867.2:c.2634+2269_2634+2273delinsGTAAC	XP_011531169.1:n.2634+2269_2634+2273delinsGTAAC
XR_001738747.2:n.2696+2269_2696+2273delinsGTAAC
XR_939685.2:n.2696+2269_2696+2273delinsGTAAC
NM_000251.3:c.*191_*195delinsGTAAC MANE Select	NP_000242.1:n.*191_*195delinsGTAAC