Canonical Allele Identifier: CA346730144

Gene: MSH2

Linked Data

• dbSNP Id: rs2104407137
• MyVariant Identifiers: chr2:g.47705588T>C (hg19) ; chr2:g.47478449T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47478449T>C , CM000664.2:g.47478449T>C	GRCh38
NC_000002.11:g.47705588T>C , CM000664.1:g.47705588T>C	GRCh37
NC_000002.10:g.47559092T>C	NCBI36
NG_007110.2:g.80326T>C , LRG_218:g.80326T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2388T>C	ENSP00000495641.2:p.Thr796=
ENST00000233146.7:c.2388T>C MANE Select	ENSP00000233146.2:p.Thr796=
ENST00000543555.6:c.2190T>C	ENSP00000442697.1:p.Thr730=
ENST00000644092.1:c.*688T>C	ENSP00000496351.1:n.*688T>C
ENST00000644900.1:c.241T>C
ENST00000645339.1:c.2388T>C	ENSP00000496441.1:p.Thr796=
ENST00000645506.1:c.2388T>C	ENSP00000495455.1:p.Thr796=
ENST00000646415.1:c.2388T>C	ENSP00000495543.1:p.Thr796=
ENST00000233146.6:c.2388T>C	ENSP00000233146.2:p.Thr796=
ENST00000406134.5:c.2388T>C	ENSP00000384199.1:p.Thr796=
ENST00000543555.5:c.2190T>C	ENSP00000442697.1:p.Thr730=
ENST00000610696.4:c.*784T>C	ENSP00000483159.1:n.*784T>C
ENST00000613514.4:c.*928T>C	ENSP00000484137.1:n.*928T>C
ENST00000617333.3:c.*1154T>C	ENSP00000482468.1:n.*1154T>C
ENST00000617938.4:c.*1360T>C	ENSP00000481158.1:n.*1360T>C
ENST00000621359.2:c.2387T>C	ENSP00000481416.1:p.Leu796Pro
NM_000251.2:c.2388T>C , LRG_218t1:c.2388T>C	NP_000242.1:p.Thr796=
NM_001258281.1:c.2190T>C	NP_001245210.1:p.Thr730=
XM_005264332.2:c.2388T>C	XP_005264389.2:p.Thr796=
XM_011532867.1:c.2388T>C	XP_011531169.1:p.Thr796=
XR_939685.1:n.2460T>C
XM_005264332.4:c.2388T>C	XP_005264389.2:p.Thr796=
XM_011532867.2:c.2388T>C	XP_011531169.1:p.Thr796=
XR_001738747.2:n.2450T>C
XR_939685.2:n.2450T>C
NM_000251.3:c.2388T>C MANE Select	NP_000242.1:p.Thr796=