Canonical Allele Identifier: CA2495877228
Gene: MSH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47482697_47482705delinsAAATGAAAC , CM000664.2:g.47482697_47482705delinsAAATGAAAC GRCh38
NC_000002.11:g.47709836_47709844delinsAAATGAAAC , CM000664.1:g.47709836_47709844delinsAAATGAAAC GRCh37
NC_000002.10:g.47563340_47563348delinsAAATGAAAC NCBI36
NG_007110.2:g.84574_84582delinsAAATGAAAC , LRG_218:g.84574_84582delinsAAATGAAAC

Transcript Alleles

HGVS Amino-acid change
ENST00000644900.2:c.2634+1826_2634+1834delinsAAATGAAAC ENSP00000495641.2:n.2634+1826_2634+1834de...
ENST00000233146.7:c.2635-82_2635-74delinsAAATGAAAC MANE Select ENSP00000233146.2:n.2635-82_2635-74delins...
ENST00000543555.6:c.2437-82_2437-74delinsAAATGAAAC ENSP00000442697.1:n.2437-82_2437-74delins...
ENST00000644092.1:c.*934+1826_*934+1834delinsAAATGAAAC ENSP00000496351.1:n.*934+1826_*934+1834de...
ENST00000644900.1:c.487+1826_487+1834delinsAAATGAAAC
ENST00000645339.1:c.2634+1826_2634+1834delinsAAATGAAAC ENSP00000496441.1:n.2634+1826_2634+1834de...
ENST00000645506.1:c.2634+1826_2634+1834delinsAAATGAAAC ENSP00000495455.1:n.2634+1826_2634+1834de...
ENST00000646415.1:c.2634+1826_2634+1834delinsAAATGAAAC ENSP00000495543.1:n.2634+1826_2634+1834de...
ENST00000233146.6:c.2635-82_2635-74delinsAAATGAAAC ENSP00000233146.2:n.2635-82_2635-74delins...
ENST00000406134.5:c.2634+1826_2634+1834delinsAAATGAAAC ENSP00000384199.1:n.2634+1826_2634+1834de...
ENST00000461394.5:n.75+1826_75+1834delinsAAATGAAAC
ENST00000543555.5:c.2437-82_2437-74delinsAAATGAAAC ENSP00000442697.1:n.2437-82_2437-74delins...
ENST00000610696.4:c.*1031-82_*1031-74delinsAAATGAAAC ENSP00000483159.1:n.*1031-82_*1031-74deli...
ENST00000613514.4:c.*1175-82_*1175-74delinsAAATGAAAC ENSP00000484137.1:n.*1175-82_*1175-74deli...
ENST00000617333.3:c.*1401-82_*1401-74delinsAAATGAAAC ENSP00000482468.1:n.*1401-82_*1401-74deli...
ENST00000617938.4:c.*1607-82_*1607-74delinsAAATGAAAC ENSP00000481158.1:n.*1607-82_*1607-74deli...
ENST00000621359.2:c.*201-82_*201-74delinsAAATGAAAC ENSP00000481416.1:n.*201-82_*201-74delins...
NM_000251.2:c.2635-82_2635-74delinsAAATGAAAC , LRG_218t1:c.2635-82_2635-74delinsAAATGAAAC NP_000242.1:n.2635-82_2635-74delinsAAATGA...
NM_001258281.1:c.2437-82_2437-74delinsAAATGAAAC NP_001245210.1:n.2437-82_2437-74delinsAAA...
XM_005264332.2:c.2634+1826_2634+1834delinsAAATGAAAC XP_005264389.2:n.2634+1826_2634+1834delin...
XM_011532867.1:c.2634+1826_2634+1834delinsAAATGAAAC XP_011531169.1:n.2634+1826_2634+1834delin...
XR_939685.1:n.2706+1826_2706+1834delinsAAATGAAAC
XM_005264332.4:c.2634+1826_2634+1834delinsAAATGAAAC XP_005264389.2:n.2634+1826_2634+1834delin...
XM_011532867.2:c.2634+1826_2634+1834delinsAAATGAAAC XP_011531169.1:n.2634+1826_2634+1834delin...
XR_001738747.2:n.2696+1826_2696+1834delinsAAATGAAAC
XR_939685.2:n.2696+1826_2696+1834delinsAAATGAAAC
NM_000251.3:c.2635-82_2635-74delinsAAATGAAAC MANE Select NP_000242.1:n.2635-82_2635-74delinsAAATGA...