Canonical Allele Identifier: CA913187905

Gene: MSH2

Linked Data

• ClinVar Variation Id: 918847
• ClinVar RCV Id: RCV001176680
• dbSNP Id: rs1672244370

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47403321_47403322delinsG , CM000664.2:g.47403321_47403322delinsG	GRCh38
NC_000002.11:g.47630460_47630461delinsG , CM000664.1:g.47630460_47630461delinsG	GRCh37
NC_000002.10:g.47483964_47483965delinsG	NCBI36
NG_007110.2:g.5198_5199delinsG , LRG_218:g.5198_5199delinsG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.130_131delinsG	ENSP00000495641.2:p.Thr44GlyfsTer20
ENST00000233146.7:c.130_131delinsG MANE Select	ENSP00000233146.2:p.Thr44GlyfsTer20
ENST00000543555.6:c.-30-39_-30-38delinsG	ENSP00000442697.1:n.-30-39_-30-38delinsG
ENST00000644092.1:c.130_131delinsG	ENSP00000496351.1:p.Thr44GlyfsTer20
ENST00000645339.1:c.130_131delinsG	ENSP00000496441.1:p.Thr44GlyfsTer20
ENST00000645506.1:c.130_131delinsG	ENSP00000495455.1:p.Thr44GlyfsTer20
ENST00000646415.1:c.130_131delinsG	ENSP00000495543.1:p.Thr44GlyfsTer20
ENST00000233146.6:c.130_131delinsG	ENSP00000233146.2:p.Thr44GlyfsTer20
ENST00000406134.5:c.130_131delinsG	ENSP00000384199.1:p.Thr44GlyfsTer20
ENST00000454849.5:c.-30-39_-30-38delinsG	ENSP00000411482.1:n.-30-39_-30-38delinsG
ENST00000543555.5:c.-30-39_-30-38delinsG	ENSP00000442697.1:n.-30-39_-30-38delinsG
ENST00000610696.4:c.130_131delinsG	ENSP00000483159.1:p.Thr44GlyfsTer20
ENST00000613514.4:c.130_131delinsG	ENSP00000484137.1:p.Thr44GlyfsTer20
ENST00000617333.3:c.130_131delinsG	ENSP00000482468.1:p.Thr44GlyfsTer20
ENST00000617938.4:c.130_131delinsG	ENSP00000481158.1:p.Thr44GlyfsTer20
ENST00000621359.2:c.130_131delinsG	ENSP00000481416.1:p.Thr44GlyfsTer20
NM_000251.2:c.130_131delinsG , LRG_218t1:c.130_131delinsG	NP_000242.1:p.Thr44GlyfsTer20
NM_001258281.1:c.-30-39_-30-38delinsG	NP_001245210.1:n.-30-39_-30-38delinsG
XM_005264332.2:c.130_131delinsG	XP_005264389.2:p.Thr44GlyfsTer20
XM_011532867.1:c.130_131delinsG	XP_011531169.1:p.Thr44GlyfsTer20
XR_939685.1:n.202_203delinsG
XM_005264332.4:c.130_131delinsG	XP_005264389.2:p.Thr44GlyfsTer20
XM_011532867.2:c.130_131delinsG	XP_011531169.1:p.Thr44GlyfsTer20
XR_001738747.2:n.192_193delinsG
XR_939685.2:n.192_193delinsG
NM_000251.3:c.130_131delinsG MANE Select	NP_000242.1:p.Thr44GlyfsTer20