Canonical Allele Identifier: CA2495872605
Gene: MSH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47475270_47475281delinsGGTAAAAAACCT , CM000664.2:g.47475270_47475281delinsGGTAAAAAACCT GRCh38
NC_000002.11:g.47702409_47702420delinsGGTAAAAAACCT , CM000664.1:g.47702409_47702420delinsGGTAAAAAACCT GRCh37
NC_000002.10:g.47555913_47555924delinsGGTAAAAAACCT NCBI36
NG_007110.2:g.77147_77158delinsGGTAAAAAACCT , LRG_218:g.77147_77158delinsGGTAAAAAACCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000644900.2:c.2005_2005+11delinsGGTAAAAAACCT
ENST00000233146.7:c.2005_2005+11delinsGGTAAAAAACCT
ENST00000543555.6:c.1807_1807+11delinsGGTAAAAAACCT
ENST00000644092.1:c.*305_*305+11delinsGGTAAAAAACCT
ENST00000645339.1:c.2005_2005+11delinsGGTAAAAAACCT
ENST00000645506.1:c.2005_2005+11delinsGGTAAAAAACCT
ENST00000646415.1:c.2005_2005+11delinsGGTAAAAAACCT
ENST00000233146.6:c.2005_2005+11delinsGGTAAAAAACCT
ENST00000406134.5:c.2005_2005+11delinsGGTAAAAAACCT
ENST00000543555.5:c.1807_1807+11delinsGGTAAAAAACCT
ENST00000610696.4:c.*401_*401+11delinsGGTAAAAAACCT
ENST00000613514.4:c.*545_*545+11delinsGGTAAAAAACCT
ENST00000617333.3:c.*771_*771+11delinsGGTAAAAAACCT
ENST00000617938.4:c.*977_*977+11delinsGGTAAAAAACCT
ENST00000621359.2:c.2005_2005+11delinsGGTAAAAAACCT
NM_000251.2:c.2005_2005+11delinsGGTAAAAAACCT , LRG_218t1:c.2005_2005+11delinsGGTAAAAAACCT
NM_001258281.1:c.1807_1807+11delinsGGTAAAAAACCT
XM_005264332.2:c.2005_2005+11delinsGGTAAAAAACCT
XM_011532867.1:c.2005_2005+11delinsGGTAAAAAACCT
XR_939685.1:n.2077_2077+11delinsGGTAAAAAACCT
XM_005264332.4:c.2005_2005+11delinsGGTAAAAAACCT
XM_011532867.2:c.2005_2005+11delinsGGTAAAAAACCT
XR_001738747.2:n.2067_2067+11delinsGGTAAAAAACCT
XR_939685.2:n.2067_2067+11delinsGGTAAAAAACCT
NM_000251.3:c.2005_2005+11delinsGGTAAAAAACCT