Canonical Allele Identifier: CA346743721
Community Standard Title: NM_000179.3(MSH6):c.1238G>T (p.Trp413Leu)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47799221G>T , CM000664.2:g.47799221G>T GRCh38
NC_000002.11:g.48026360G>T , CM000664.1:g.48026360G>T GRCh37
NC_000002.10:g.47879864G>T NCBI36
NG_007111.1:g.21075G>T , LRG_219:g.21075G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000179.3:c.1238G>T (MSH6) MANE Select NP_000170.1:p.Trp413Leu
ENST00000234420.11:c.1238G>T (MSH6) MANE Select ENSP00000234420.5:p.Trp413Leu
NM_000179.2:c.1238G>T , LRG_219t1:c.1238G>T (MSH6) NP_000170.1:p.Trp413Leu
NM_001281492.1:c.848G>T (MSH6) NP_001268421.1:p.Trp283Leu
NM_001281492.2:c.848G>T (MSH6) NP_001268421.1:p.Trp283Leu
NM_001281493.1:c.332G>T (MSH6) NP_001268422.1:p.Trp111Leu
NM_001281493.2:c.332G>T (MSH6) NP_001268422.1:p.Trp111Leu
NM_001281494.1:c.332G>T (MSH6) NP_001268423.1:p.Trp111Leu
NM_001281494.2:c.332G>T (MSH6) NP_001268423.1:p.Trp111Leu
ENST00000234420.9:c.1238G>T (MSH6) ENSP00000234420.4:p.Trp413Leu
ENST00000405808.5:c.169+8974C>A (FBXO11) ENSP00000385127.1:n.169+8974C>A
ENST00000411819.2:c.941G>T (MSH6) ENSP00000406248.2:p.Trp314Leu
ENST00000420813.6:c.941G>T (MSH6) ENSP00000390382.2:p.Trp314Leu
ENST00000434234.5:c.*124+8773C>A (FBXO11) ENSP00000402692.1:n.*124+8773C>A
ENST00000445503.5:c.*585G>T (MSH6) ENSP00000405294.1:n.*585G>T
ENST00000455383.6:c.941G>T (MSH6) ENSP00000397484.2:p.Trp314Leu
ENST00000538136.1:c.332G>T (MSH6) ENSP00000438580.1:p.Trp111Leu
ENST00000540021.5:c.848G>T (MSH6) ENSP00000446475.1:p.Trp283Leu
ENST00000540021.6:c.848G>T (MSH6) ENSP00000446475.1:p.Trp283Leu
ENST00000614496.4:c.332G>T (MSH6) ENSP00000477844.1:p.Trp111Leu
ENST00000616033.4:c.1235G>T (MSH6) ENSP00000480261.1:p.Trp412Leu
ENST00000622629.4:c.-1859G>T (MSH6) ENSP00000482078.1:n.-1859G>T
ENST00000652107.1:c.941G>T (MSH6) ENSP00000498629.1:p.Trp314Leu
ENST00000673637.1:c.941G>T (MSH6) ENSP00000501310.1:p.Trp314Leu
ENST00000699999.1:n.1322G>T (MSH6)
ENST00000700000.1:c.1238G>T (MSH6) ENSP00000514749.1:p.Trp413Leu
ENST00000700002.1:c.1244G>T (MSH6) ENSP00000514750.1:p.Trp415Leu
ENST00000700003.1:c.627+3158G>T (MSH6) ENSP00000514751.1:n.627+3158G>T
ENST00000700004.1:c.395G>T (MSH6) ENSP00000514752.1:p.Trp132Leu
ENST00000700004.2:c.1238G>T (MSH6) ENSP00000514752.2:p.Trp413Leu
XM_005264271.1:c.941G>T (MSH6) XP_005264328.1:p.Trp314Leu
XM_011532798.1:c.1055G>T (MSH6) XP_011531100.1:p.Trp352Leu
XM_011532799.1:c.941G>T (MSH6) XP_011531101.1:p.Trp314Leu
XM_011532800.1:c.941G>T (MSH6) XP_011531102.1:p.Trp314Leu
XM_024452819.1:c.1238G>T (MSH6) XP_024308587.1:p.Trp413Leu
XM_024452820.1:c.1055G>T (MSH6) XP_024308588.1:p.Trp352Leu
XM_024452821.1:c.941G>T (MSH6) XP_024308589.1:p.Trp314Leu
XM_024452822.1:c.332G>T (MSH6) XP_024308590.1:p.Trp111Leu