Canonical Allele Identifier: CA346740355

Linked Data

ClinVar Variation Id: 479870
ClinVar RCV Id: RCV000564981
dbSNP Id: rs1553412223

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47798788A>T , CM000664.2:g.47798788A>T GRCh38
NC_000002.11:g.48025927A>T , CM000664.1:g.48025927A>T GRCh37
NC_000002.10:g.47879431A>T NCBI36
NG_007111.1:g.20642A>T , LRG_219:g.20642A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000411819.2:c.508A>T (MSH6) ENSP00000406248.2:p.Thr170Ser
ENST00000420813.6:c.508A>T (MSH6) ENSP00000390382.2:p.Thr170Ser
ENST00000455383.6:c.508A>T (MSH6) ENSP00000397484.2:p.Thr170Ser
ENST00000700004.2:c.805A>T (MSH6) ENSP00000514752.2:p.Thr269Ser
ENST00000699999.1:n.889A>T (MSH6)
ENST00000700000.1:c.805A>T (MSH6) ENSP00000514749.1:p.Thr269Ser
ENST00000700002.1:c.811A>T (MSH6) ENSP00000514750.1:p.Thr271Ser
ENST00000700003.1:c.627+2725A>T (MSH6) ENSP00000514751.1:n.627+2725A>T
ENST00000234420.11:c.805A>T (MSH6) MANE Select ENSP00000234420.5:p.Thr269Ser
ENST00000540021.6:c.415A>T (MSH6) ENSP00000446475.1:p.Thr139Ser
ENST00000652107.1:c.508A>T (MSH6) ENSP00000498629.1:p.Thr170Ser
ENST00000673637.1:c.508A>T (MSH6) ENSP00000501310.1:p.Thr170Ser
ENST00000673922.1:n.527A>T (MSH6)
ENST00000234420.9:c.805A>T (MSH6) ENSP00000234420.4:p.Thr269Ser
ENST00000405808.5:c.170-9348T>A (FBXO11) ENSP00000385127.1:n.170-9348T>A
ENST00000434234.5:c.*124+9206T>A (FBXO11) ENSP00000402692.1:n.*124+9206T>A
ENST00000445503.5:c.*152A>T (MSH6) ENSP00000405294.1:n.*152A>T
ENST00000456246.1:c.*293A>T (MSH6) ENSP00000410570.1:n.*293A>T
ENST00000538136.1:c.-102A>T (MSH6) ENSP00000438580.1:n.-102A>T
ENST00000540021.5:c.415A>T (MSH6) ENSP00000446475.1:p.Thr139Ser
ENST00000614496.4:c.-102A>T (MSH6) ENSP00000477844.1:n.-102A>T
ENST00000616033.4:c.802A>T (MSH6) ENSP00000480261.1:p.Thr268Ser
ENST00000622629.4:c.-2292A>T (MSH6) ENSP00000482078.1:n.-2292A>T
NM_000179.2:c.805A>T , LRG_219t1:c.805A>T (MSH6) NP_000170.1:p.Thr269Ser
NM_001281492.1:c.415A>T (MSH6) NP_001268421.1:p.Thr139Ser
NM_001281493.1:c.-102A>T (MSH6) NP_001268422.1:n.-102A>T
NM_001281494.1:c.-102A>T (MSH6) NP_001268423.1:n.-102A>T
XM_005264271.1:c.508A>T (MSH6) XP_005264328.1:p.Thr170Ser
XM_011532798.1:c.622A>T (MSH6) XP_011531100.1:p.Thr208Ser
XM_011532799.1:c.508A>T (MSH6) XP_011531101.1:p.Thr170Ser
XM_011532800.1:c.508A>T (MSH6) XP_011531102.1:p.Thr170Ser
XM_024452819.1:c.805A>T (MSH6) XP_024308587.1:p.Thr269Ser
XM_024452820.1:c.622A>T (MSH6) XP_024308588.1:p.Thr208Ser
XM_024452821.1:c.508A>T (MSH6) XP_024308589.1:p.Thr170Ser
XM_024452822.1:c.-102A>T (MSH6) XP_024308590.1:n.-102A>T
NM_000179.3:c.805A>T (MSH6) MANE Select NP_000170.1:p.Thr269Ser
NM_001281492.2:c.415A>T (MSH6) NP_001268421.1:p.Thr139Ser
NM_001281493.2:c.-102A>T (MSH6) NP_001268422.1:n.-102A>T
NM_001281494.2:c.-102A>T (MSH6) NP_001268423.1:n.-102A>T