Canonical Allele Identifier: CA2495874630

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47478466_47478468delinsTCA , CM000664.2:g.47478466_47478468delinsTCA	GRCh38
NC_000002.11:g.47705605_47705607delinsTCA , CM000664.1:g.47705605_47705607delinsTCA	GRCh37
NC_000002.10:g.47559109_47559111delinsTCA	NCBI36
NG_007110.2:g.80343_80345delinsTCA , LRG_218:g.80343_80345delinsTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2405_2407delinsTCA	ENSP00000495641.2:p.Val802=
ENST00000233146.7:c.2405_2407delinsTCA MANE Select	ENSP00000233146.2:p.Val802=
ENST00000543555.6:c.2207_2209delinsTCA	ENSP00000442697.1:p.Val736=
ENST00000644092.1:c.*705_*707delinsTCA	ENSP00000496351.1:n.*705_*707delinsTCA
ENST00000644900.1:c.258_260delinsTCA
ENST00000645339.1:c.2405_2407delinsTCA	ENSP00000496441.1:p.Val802=
ENST00000645506.1:c.2405_2407delinsTCA	ENSP00000495455.1:p.Val802=
ENST00000646415.1:c.2405_2407delinsTCA	ENSP00000495543.1:p.Val802=
ENST00000233146.6:c.2405_2407delinsTCA	ENSP00000233146.2:p.Val802=
ENST00000406134.5:c.2405_2407delinsTCA	ENSP00000384199.1:p.Val802=
ENST00000543555.5:c.2207_2209delinsTCA	ENSP00000442697.1:p.Val736=
ENST00000610696.4:c.*801_*803delinsTCA	ENSP00000483159.1:n.*801_*803delinsTCA
ENST00000613514.4:c.*945_*947delinsTCA	ENSP00000484137.1:n.*945_*947delinsTCA
ENST00000617333.3:c.*1171_*1173delinsTCA	ENSP00000482468.1:n.*1171_*1173delinsTCA
ENST00000617938.4:c.*1377_*1379delinsTCA	ENSP00000481158.1:n.*1377_*1379delinsTCA
ENST00000621359.2:c.2404_2406delinsTCA	ENSP00000481416.1:p.Ser802=
NM_000251.2:c.2405_2407delinsTCA , LRG_218t1:c.2405_2407delinsTCA	NP_000242.1:p.Val802=
NM_001258281.1:c.2207_2209delinsTCA	NP_001245210.1:p.Val736=
XM_005264332.2:c.2405_2407delinsTCA	XP_005264389.2:p.Val802=
XM_011532867.1:c.2405_2407delinsTCA	XP_011531169.1:p.Val802=
XR_939685.1:n.2477_2479delinsTCA
XM_005264332.4:c.2405_2407delinsTCA	XP_005264389.2:p.Val802=
XM_011532867.2:c.2405_2407delinsTCA	XP_011531169.1:p.Val802=
XR_001738747.2:n.2467_2469delinsTCA
XR_939685.2:n.2467_2469delinsTCA
NM_000251.3:c.2405_2407delinsTCA MANE Select	NP_000242.1:p.Val802=