Canonical Allele Identifier: CA346745060

Linked Data

ClinVar Variation Id: 2162051
ClinVar RCV Id: RCV003078884
dbSNP Id: rs864622435

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47799370G>A , CM000664.2:g.47799370G>A GRCh38
NC_000002.11:g.48026509G>A , CM000664.1:g.48026509G>A GRCh37
NC_000002.10:g.47880013G>A NCBI36
NG_007111.1:g.21224G>A , LRG_219:g.21224G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000411819.2:c.1090G>A (MSH6) ENSP00000406248.2:p.Glu364Lys
ENST00000420813.6:c.1090G>A (MSH6) ENSP00000390382.2:p.Glu364Lys
ENST00000455383.6:c.1090G>A (MSH6) ENSP00000397484.2:p.Glu364Lys
ENST00000700004.2:c.1387G>A (MSH6) ENSP00000514752.2:p.Glu463Lys
ENST00000699999.1:n.1471G>A (MSH6)
ENST00000700000.1:c.1387G>A (MSH6) ENSP00000514749.1:p.Glu463Lys
ENST00000700002.1:c.1393G>A (MSH6) ENSP00000514750.1:p.Glu465Lys
ENST00000700003.1:c.627+3307G>A (MSH6) ENSP00000514751.1:n.627+3307G>A
ENST00000700004.1:c.544G>A (MSH6) ENSP00000514752.1:p.Glu182Lys
ENST00000234420.11:c.1387G>A (MSH6) MANE Select ENSP00000234420.5:p.Glu463Lys
ENST00000540021.6:c.997G>A (MSH6) ENSP00000446475.1:p.Glu333Lys
ENST00000652107.1:c.1090G>A (MSH6) ENSP00000498629.1:p.Glu364Lys
ENST00000673637.1:c.1090G>A (MSH6) ENSP00000501310.1:p.Glu364Lys
ENST00000234420.9:c.1387G>A (MSH6) ENSP00000234420.4:p.Glu463Lys
ENST00000405808.5:c.169+8825C>T (FBXO11) ENSP00000385127.1:n.169+8825C>T
ENST00000434234.5:c.*124+8624C>T (FBXO11) ENSP00000402692.1:n.*124+8624C>T
ENST00000445503.5:c.*734G>A (MSH6) ENSP00000405294.1:n.*734G>A
ENST00000538136.1:c.481G>A (MSH6) ENSP00000438580.1:p.Glu161Lys
ENST00000540021.5:c.997G>A (MSH6) ENSP00000446475.1:p.Glu333Lys
ENST00000614496.4:c.481G>A (MSH6) ENSP00000477844.1:p.Glu161Lys
ENST00000616033.4:c.1384G>A (MSH6) ENSP00000480261.1:p.Glu462Lys
ENST00000622629.4:c.-1710G>A (MSH6) ENSP00000482078.1:n.-1710G>A
NM_000179.2:c.1387G>A , LRG_219t1:c.1387G>A (MSH6) NP_000170.1:p.Glu463Lys
NM_001281492.1:c.997G>A (MSH6) NP_001268421.1:p.Glu333Lys
NM_001281493.1:c.481G>A (MSH6) NP_001268422.1:p.Glu161Lys
NM_001281494.1:c.481G>A (MSH6) NP_001268423.1:p.Glu161Lys
XM_005264271.1:c.1090G>A (MSH6) XP_005264328.1:p.Glu364Lys
XM_011532798.1:c.1204G>A (MSH6) XP_011531100.1:p.Glu402Lys
XM_011532799.1:c.1090G>A (MSH6) XP_011531101.1:p.Glu364Lys
XM_011532800.1:c.1090G>A (MSH6) XP_011531102.1:p.Glu364Lys
XM_024452819.1:c.1387G>A (MSH6) XP_024308587.1:p.Glu463Lys
XM_024452820.1:c.1204G>A (MSH6) XP_024308588.1:p.Glu402Lys
XM_024452821.1:c.1090G>A (MSH6) XP_024308589.1:p.Glu364Lys
XM_024452822.1:c.481G>A (MSH6) XP_024308590.1:p.Glu161Lys
NM_000179.3:c.1387G>A (MSH6) MANE Select NP_000170.1:p.Glu463Lys
NM_001281492.2:c.997G>A (MSH6) NP_001268421.1:p.Glu333Lys
NM_001281493.2:c.481G>A (MSH6) NP_001268422.1:p.Glu161Lys
NM_001281494.2:c.481G>A (MSH6) NP_001268423.1:p.Glu161Lys