Canonical Allele Identifier: CA346746028
Gene: MSH6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47799463G>A , CM000664.2:g.47799463G>A GRCh38
NC_000002.11:g.48026602G>A , CM000664.1:g.48026602G>A GRCh37
NC_000002.10:g.47880106G>A NCBI36
NG_007111.1:g.21317G>A , LRG_219:g.21317G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000234420.11:c.1480G>A MANE Select ENSP00000234420.5:p.Ala494Thr
ENST00000540021.6:c.1090G>A ENSP00000446475.1:p.Ala364Thr
ENST00000652107.1:c.1183G>A ENSP00000498629.1:p.Ala395Thr
ENST00000673637.1:c.1183G>A ENSP00000501310.1:p.Ala395Thr
ENST00000234420.9:c.1480G>A ENSP00000234420.4:p.Ala494Thr
ENST00000405808.5:c.169+8732C>T ENSP00000385127.1:p.=
ENST00000434234.5:c.*124+8531C>T ENSP00000402692.1:p.=
ENST00000445503.5:c.*827G>A ENSP00000405294.1:p.=
ENST00000538136.1:c.574G>A ENSP00000438580.1:p.Ala192Thr
ENST00000540021.5:c.1090G>A ENSP00000446475.1:p.Ala364Thr
ENST00000614496.4:c.574G>A ENSP00000477844.1:p.Ala192Thr
ENST00000616033.4:c.1477G>A ENSP00000480261.1:p.Ala493Thr
ENST00000622629.4:c.-1617G>A ENSP00000482078.1:p.=
NM_000179.2:c.1480G>A , LRG_219t1:c.1480G>A NP_000170.1:p.Ala494Thr
NM_001281492.1:c.1090G>A NP_001268421.1:p.Ala364Thr
NM_001281493.1:c.574G>A NP_001268422.1:p.Ala192Thr
NM_001281494.1:c.574G>A NP_001268423.1:p.Ala192Thr
XM_005264271.1:c.1183G>A XP_005264328.1:p.Ala395Thr
XM_011532798.1:c.1297G>A XP_011531100.1:p.Ala433Thr
XM_011532799.1:c.1183G>A XP_011531101.1:p.Ala395Thr
XM_011532800.1:c.1183G>A XP_011531102.1:p.Ala395Thr
XM_024452819.1:c.1480G>A XP_024308587.1:p.Ala494Thr
XM_024452820.1:c.1297G>A XP_024308588.1:p.Ala433Thr
XM_024452821.1:c.1183G>A XP_024308589.1:p.Ala395Thr
XM_024452822.1:c.574G>A XP_024308590.1:p.Ala192Thr
NM_000179.3:c.1480G>A MANE Select NP_000170.1:p.Ala494Thr
NM_001281492.2:c.1090G>A NP_001268421.1:p.Ala364Thr
NM_001281493.2:c.574G>A NP_001268422.1:p.Ala192Thr
NM_001281494.2:c.574G>A NP_001268423.1:p.Ala192Thr