Canonical Allele Identifier: CA346746061
Gene: MSH6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47799467G>C , CM000664.2:g.47799467G>C GRCh38
NC_000002.11:g.48026606G>C , CM000664.1:g.48026606G>C GRCh37
NC_000002.10:g.47880110G>C NCBI36
NG_007111.1:g.21321G>C , LRG_219:g.21321G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000234420.11:c.1484G>C MANE Select ENSP00000234420.5:p.Arg495Pro
ENST00000540021.6:c.1094G>C ENSP00000446475.1:p.Arg365Pro
ENST00000652107.1:c.1187G>C ENSP00000498629.1:p.Arg396Pro
ENST00000673637.1:c.1187G>C ENSP00000501310.1:p.Arg396Pro
ENST00000234420.9:c.1484G>C ENSP00000234420.4:p.Arg495Pro
ENST00000405808.5:c.169+8728C>G ENSP00000385127.1:p.=
ENST00000434234.5:c.*124+8527C>G ENSP00000402692.1:p.=
ENST00000445503.5:c.*831G>C ENSP00000405294.1:p.=
ENST00000538136.1:c.578G>C ENSP00000438580.1:p.Arg193Pro
ENST00000540021.5:c.1094G>C ENSP00000446475.1:p.Arg365Pro
ENST00000614496.4:c.578G>C ENSP00000477844.1:p.Arg193Pro
ENST00000616033.4:c.1481G>C ENSP00000480261.1:p.Arg494Pro
ENST00000622629.4:c.-1613G>C ENSP00000482078.1:p.=
NM_000179.2:c.1484G>C , LRG_219t1:c.1484G>C NP_000170.1:p.Arg495Pro
NM_001281492.1:c.1094G>C NP_001268421.1:p.Arg365Pro
NM_001281493.1:c.578G>C NP_001268422.1:p.Arg193Pro
NM_001281494.1:c.578G>C NP_001268423.1:p.Arg193Pro
XM_005264271.1:c.1187G>C XP_005264328.1:p.Arg396Pro
XM_011532798.1:c.1301G>C XP_011531100.1:p.Arg434Pro
XM_011532799.1:c.1187G>C XP_011531101.1:p.Arg396Pro
XM_011532800.1:c.1187G>C XP_011531102.1:p.Arg396Pro
XM_024452819.1:c.1484G>C XP_024308587.1:p.Arg495Pro
XM_024452820.1:c.1301G>C XP_024308588.1:p.Arg434Pro
XM_024452821.1:c.1187G>C XP_024308589.1:p.Arg396Pro
XM_024452822.1:c.578G>C XP_024308590.1:p.Arg193Pro
NM_000179.3:c.1484G>C MANE Select NP_000170.1:p.Arg495Pro
NM_001281492.2:c.1094G>C NP_001268421.1:p.Arg365Pro
NM_001281493.2:c.578G>C NP_001268422.1:p.Arg193Pro
NM_001281494.2:c.578G>C NP_001268423.1:p.Arg193Pro