Canonical Allele Identifier: CA071830

Linked Data

ClinVar Variation Id: 638837
dbSNP Id: rs63750370
gnomAD v2: 2-48033370-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47806231C>A , CM000664.2:g.47806231C>A GRCh38
NC_000002.11:g.48033370C>A , CM000664.1:g.48033370C>A GRCh37
NC_000002.10:g.47886874C>A NCBI36
NG_007111.1:g.28085C>A , LRG_219:g.28085C>A
NG_008397.1:g.104445G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000411819.2:c.3377C>A (MSH6) ENSP00000406248.2:p.Thr1126Lys
ENST00000420813.6:c.3377C>A (MSH6) ENSP00000390382.2:p.Thr1126Lys
ENST00000455383.6:c.3377C>A (MSH6) ENSP00000397484.2:p.Thr1126Lys
ENST00000700004.2:c.3290C>A (MSH6) ENSP00000514752.2:p.Thr1097Lys
ENST00000699999.1:n.4348C>A (MSH6)
ENST00000700000.1:c.2108C>A (MSH6) ENSP00000514749.1:p.Thr703Lys
ENST00000700002.1:c.3680C>A (MSH6) ENSP00000514750.1:p.Thr1227Lys
ENST00000700003.1:c.1129C>A (MSH6) ENSP00000514751.1:n.1129C>A
ENST00000700004.1:c.2447C>A (MSH6) ENSP00000514752.1:p.Thr816Lys
ENST00000700005.1:n.2525C>A (MSH6)
ENST00000700006.1:n.4832C>A (MSH6)
ENST00000700007.1:n.2269C>A (MSH6)
ENST00000700008.1:n.1843C>A (MSH6)
ENST00000700009.1:n.2338C>A (MSH6)
ENST00000700010.1:n.1083C>A (MSH6)
ENST00000700011.1:n.2968C>A (MSH6)
ENST00000682451.1:n.4517G>T (FBXO11)
ENST00000684712.1:n.4779G>T (FBXO11)
ENST00000234420.11:c.3674C>A (MSH6) MANE Select ENSP00000234420.5:p.Thr1225Lys
ENST00000540021.6:c.3284C>A (MSH6) ENSP00000446475.1:p.Thr1095Lys
ENST00000652107.1:c.3377C>A (MSH6) ENSP00000498629.1:p.Thr1126Lys
ENST00000673637.1:c.3377C>A (MSH6) ENSP00000501310.1:p.Thr1126Lys
ENST00000234420.9:c.3674C>A (MSH6) ENSP00000234420.4:p.Thr1225Lys
ENST00000405808.5:c.169+1964G>T (FBXO11) ENSP00000385127.1:n.169+1964G>T
ENST00000434234.5:c.*124+1763G>T (FBXO11) ENSP00000402692.1:n.*124+1763G>T
ENST00000445503.5:c.*3021C>A (MSH6) ENSP00000405294.1:n.*3021C>A
ENST00000538136.1:c.2768C>A (MSH6) ENSP00000438580.1:p.Thr923Lys
ENST00000540021.5:c.3284C>A (MSH6) ENSP00000446475.1:p.Thr1095Lys
ENST00000614496.4:c.2768C>A (MSH6) ENSP00000477844.1:p.Thr923Lys
ENST00000622629.4:c.578C>A (MSH6) ENSP00000482078.1:p.Thr193Lys
NM_000179.2:c.3674C>A , LRG_219t1:c.3674C>A (MSH6) NP_000170.1:p.Thr1225Lys
NM_001281492.1:c.3284C>A (MSH6) NP_001268421.1:p.Thr1095Lys
NM_001281493.1:c.2768C>A (MSH6) NP_001268422.1:p.Thr923Lys
NM_001281494.1:c.2768C>A (MSH6) NP_001268423.1:p.Thr923Lys
XM_005264271.1:c.3377C>A (MSH6) XP_005264328.1:p.Thr1126Lys
XM_011532798.1:c.3491C>A (MSH6) XP_011531100.1:p.Thr1164Lys
XM_011532799.1:c.3377C>A (MSH6) XP_011531101.1:p.Thr1126Lys
XM_011532800.1:c.3377C>A (MSH6) XP_011531102.1:p.Thr1126Lys
XM_024452819.1:c.3674C>A (MSH6) XP_024308587.1:p.Thr1225Lys
XM_024452820.1:c.3491C>A (MSH6) XP_024308588.1:p.Thr1164Lys
XM_024452821.1:c.3377C>A (MSH6) XP_024308589.1:p.Thr1126Lys
XM_024452822.1:c.2768C>A (MSH6) XP_024308590.1:p.Thr923Lys
NM_000179.3:c.3674C>A (MSH6) MANE Select NP_000170.1:p.Thr1225Lys
NM_001281492.2:c.3284C>A (MSH6) NP_001268421.1:p.Thr1095Lys
NM_001281493.2:c.2768C>A (MSH6) NP_001268422.1:p.Thr923Lys
NM_001281494.2:c.2768C>A (MSH6) NP_001268423.1:p.Thr923Lys