Canonical Allele Identifier: CA2580066995

Gene: MSH2

Linked Data

• ClinVar Variation Id: 1780983
• ClinVar RCV Id: RCV002412670

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47475097dup , CM000664.2:g.47475097dup	GRCh38
NC_000002.11:g.47702236dup , CM000664.1:g.47702236dup	GRCh37
NC_000002.10:g.47555740dup	NCBI36
NG_007110.2:g.76974dup , LRG_218:g.76974dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.1832dup	ENSP00000495641.2:p.Ser612ValfsTer?
ENST00000233146.7:c.1832dup MANE Select	ENSP00000233146.2:p.Ser612ValfsTer?
ENST00000543555.6:c.1634dup	ENSP00000442697.1:p.Ser546ValfsTer?
ENST00000644092.1:c.*132dup	ENSP00000496351.1:n.*132dup
ENST00000645339.1:c.1832dup	ENSP00000496441.1:p.Ser612ValfsTer?
ENST00000645506.1:c.1832dup	ENSP00000495455.1:p.Ser612ValfsTer?
ENST00000646415.1:c.1832dup	ENSP00000495543.1:p.Ser612ValfsTer?
ENST00000233146.6:c.1832dup	ENSP00000233146.2:p.Ser612ValfsTer?
ENST00000406134.5:c.1832dup	ENSP00000384199.1:p.Ser612ValfsTer?
ENST00000543555.5:c.1634dup	ENSP00000442697.1:p.Ser546ValfsTer?
ENST00000610696.4:c.*228dup	ENSP00000483159.1:n.*228dup
ENST00000613514.4:c.*372dup	ENSP00000484137.1:n.*372dup
ENST00000617333.3:c.*598dup	ENSP00000482468.1:n.*598dup
ENST00000617938.4:c.*804dup	ENSP00000481158.1:n.*804dup
ENST00000621359.2:c.1832dup	ENSP00000481416.1:p.Ser612ValfsTer?
NM_000251.2:c.1832dup , LRG_218t1:c.1832dup	NP_000242.1:p.Ser612ValfsTer?
NM_001258281.1:c.1634dup	NP_001245210.1:p.Ser546ValfsTer?
XM_005264332.2:c.1832dup	XP_005264389.2:p.Ser612ValfsTer?
XM_011532867.1:c.1832dup	XP_011531169.1:p.Ser612ValfsTer?
XR_939685.1:n.1904dup
XM_005264332.4:c.1832dup	XP_005264389.2:p.Ser612ValfsTer?
XM_011532867.2:c.1832dup	XP_011531169.1:p.Ser612ValfsTer?
XR_001738747.2:n.1894dup
XR_939685.2:n.1894dup
NM_000251.3:c.1832dup MANE Select	NP_000242.1:p.Ser612ValfsTer?