Canonical Allele Identifier: CA2495830075

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47408398_47408401delinsAAGG , CM000664.2:g.47408398_47408401delinsAAGG	GRCh38
NC_000002.11:g.47635537_47635540delinsAAGG , CM000664.1:g.47635537_47635540delinsAAGG	GRCh37
NC_000002.10:g.47489041_47489044delinsAAGG	NCBI36
NG_007110.2:g.10275_10278delinsAAGG , LRG_218:g.10275_10278delinsAAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.212-3_212delinsAAGG
ENST00000233146.7:c.212-3_212delinsAAGG
ENST00000543555.6:c.14-3_14delinsAAGG
ENST00000644092.1:c.212-3_212delinsAAGG
ENST00000645339.1:c.212-3_212delinsAAGG
ENST00000645506.1:c.212-3_212delinsAAGG
ENST00000646415.1:c.212-3_212delinsAAGG
ENST00000233146.6:c.212-3_212delinsAAGG
ENST00000406134.5:c.212-3_212delinsAAGG
ENST00000454849.5:c.14-3_14delinsAAGG
ENST00000543555.5:c.14-3_14delinsAAGG
ENST00000610696.4:c.212-3_212delinsAAGG
ENST00000613514.4:c.212-3_212delinsAAGG
ENST00000617333.3:c.212-3_212delinsAAGG
ENST00000617938.4:c.212-3_212delinsAAGG
ENST00000621359.2:c.212-3_212delinsAAGG
NM_000251.2:c.212-3_212delinsAAGG , LRG_218t1:c.212-3_212delinsAAGG
NM_001258281.1:c.14-3_14delinsAAGG
XM_005264332.2:c.212-3_212delinsAAGG
XM_011532867.1:c.212-3_212delinsAAGG
XR_939685.1:n.284-3_284delinsAAGG
XM_005264332.4:c.212-3_212delinsAAGG
XM_011532867.2:c.212-3_212delinsAAGG
XR_001738747.2:n.274-3_274delinsAAGG
XR_939685.2:n.274-3_274delinsAAGG
NM_000251.3:c.212-3_212delinsAAGG