Canonical Allele Identifier: CA645531408

Gene: MSH2

Linked Data

• COSMIC: COSM5967498

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47408402_47408419del , CM000664.2:g.47408402_47408419del	GRCh38
NC_000002.11:g.47635541_47635558del , CM000664.1:g.47635541_47635558del	GRCh37
NC_000002.10:g.47489045_47489062del	NCBI36
NG_007110.2:g.10279_10296del , LRG_218:g.10279_10296del

Transcript Alleles

HGVS	Amino-acid change
ENST00000644900.2:c.213_230del	ENSP00000495641.2:p.Ala72_Ser77del
ENST00000233146.7:c.213_230del MANE Select	ENSP00000233146.2:p.Ala72_Ser77del
ENST00000543555.6:c.15_32del	ENSP00000442697.1:p.Ala6_Ser11del
ENST00000644092.1:c.213_230del	ENSP00000496351.1:p.Ala72_Ser77del
ENST00000645339.1:c.213_230del	ENSP00000496441.1:p.Ala72_Ser77del
ENST00000645506.1:c.213_230del	ENSP00000495455.1:p.Ala72_Ser77del
ENST00000646415.1:c.213_230del	ENSP00000495543.1:p.Ala72_Ser77del
ENST00000233146.6:c.213_230del	ENSP00000233146.2:p.Ala72_Ser77del
ENST00000406134.5:c.213_230del	ENSP00000384199.1:p.Ala72_Ser77del
ENST00000454849.5:c.15_32del	ENSP00000411482.1:p.Ala6_Ser11del
ENST00000543555.5:c.15_32del	ENSP00000442697.1:p.Ala6_Ser11del
ENST00000610696.4:c.213_230del	ENSP00000483159.1:p.Ala72_Ser77del
ENST00000613514.4:c.213_230del	ENSP00000484137.1:p.Ala72_Ser77del
ENST00000617333.3:c.213_230del	ENSP00000482468.1:p.Ala72_Ser77del
ENST00000617938.4:c.213_230del	ENSP00000481158.1:p.Ala72_Ser77del
ENST00000621359.2:c.213_230del	ENSP00000481416.1:p.Ala72_Ser77del
NM_000251.2:c.213_230del , LRG_218t1:c.213_230del	NP_000242.1:p.Ala72_Ser77del
NM_001258281.1:c.15_32del	NP_001245210.1:p.Ala6_Ser11del
XM_005264332.2:c.213_230del	XP_005264389.2:p.Ala72_Ser77del
XM_011532867.1:c.213_230del	XP_011531169.1:p.Ala72_Ser77del
XR_939685.1:n.285_302del
XM_005264332.4:c.213_230del	XP_005264389.2:p.Ala72_Ser77del
XM_011532867.2:c.213_230del	XP_011531169.1:p.Ala72_Ser77del
XR_001738747.2:n.275_292del
XR_939685.2:n.275_292del
NM_000251.3:c.213_230del MANE Select	NP_000242.1:p.Ala72_Ser77del