Canonical Allele Identifier: CA2495872581
Gene: MSH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47475247_47475249delinsAAC , CM000664.2:g.47475247_47475249delinsAAC GRCh38
NC_000002.11:g.47702386_47702388delinsAAC , CM000664.1:g.47702386_47702388delinsAAC GRCh37
NC_000002.10:g.47555890_47555892delinsAAC NCBI36
NG_007110.2:g.77124_77126delinsAAC , LRG_218:g.77124_77126delinsAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000644900.2:c.1982_1984delinsAAC ENSP00000495641.2:p.Lys661=
ENST00000233146.7:c.1982_1984delinsAAC MANE Select ENSP00000233146.2:p.Lys661=
ENST00000543555.6:c.1784_1786delinsAAC ENSP00000442697.1:p.Lys595=
ENST00000644092.1:c.*282_*284delinsAAC ENSP00000496351.1:n.*282_*284delinsAAC
ENST00000645339.1:c.1982_1984delinsAAC ENSP00000496441.1:p.Lys661=
ENST00000645506.1:c.1982_1984delinsAAC ENSP00000495455.1:p.Lys661=
ENST00000646415.1:c.1982_1984delinsAAC ENSP00000495543.1:p.Lys661=
ENST00000233146.6:c.1982_1984delinsAAC ENSP00000233146.2:p.Lys661=
ENST00000406134.5:c.1982_1984delinsAAC ENSP00000384199.1:p.Lys661=
ENST00000543555.5:c.1784_1786delinsAAC ENSP00000442697.1:p.Lys595=
ENST00000610696.4:c.*378_*380delinsAAC ENSP00000483159.1:n.*378_*380delinsAAC
ENST00000613514.4:c.*522_*524delinsAAC ENSP00000484137.1:n.*522_*524delinsAAC
ENST00000617333.3:c.*748_*750delinsAAC ENSP00000482468.1:n.*748_*750delinsAAC
ENST00000617938.4:c.*954_*956delinsAAC ENSP00000481158.1:n.*954_*956delinsAAC
ENST00000621359.2:c.1982_1984delinsAAC ENSP00000481416.1:p.Lys661=
NM_000251.2:c.1982_1984delinsAAC , LRG_218t1:c.1982_1984delinsAAC NP_000242.1:p.Lys661=
NM_001258281.1:c.1784_1786delinsAAC NP_001245210.1:p.Lys595=
XM_005264332.2:c.1982_1984delinsAAC XP_005264389.2:p.Lys661=
XM_011532867.1:c.1982_1984delinsAAC XP_011531169.1:p.Lys661=
XR_939685.1:n.2054_2056delinsAAC
XM_005264332.4:c.1982_1984delinsAAC XP_005264389.2:p.Lys661=
XM_011532867.2:c.1982_1984delinsAAC XP_011531169.1:p.Lys661=
XR_001738747.2:n.2044_2046delinsAAC
XR_939685.2:n.2044_2046delinsAAC
NM_000251.3:c.1982_1984delinsAAC MANE Select NP_000242.1:p.Lys661=