Canonical Allele Identifier: CA2496038165
Gene: MSH6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47783379C= , CM000664.2:g.47783379C= GRCh38
NC_000002.11:g.48010518C= , CM000664.1:g.48010518C= GRCh37
NC_000002.10:g.47864022C= NCBI36
NG_007111.1:g.5233C= , LRG_219:g.5233C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700004.2:c.146C= ENSP00000514752.2:p.Ala49=
ENST00000699999.1:n.230C=
ENST00000700000.1:c.146C= ENSP00000514749.1:p.Ala49=
ENST00000700001.1:n.218C=
ENST00000700002.1:c.146C= ENSP00000514750.1:p.Ala49=
ENST00000700003.1:c.146C= ENSP00000514751.1:p.Ala49=
ENST00000234420.11:c.146C= MANE Select ENSP00000234420.5:p.Ala49=
ENST00000540021.6:c.146C= ENSP00000446475.1:p.Ala49=
ENST00000652107.1:c.-37-7548C= ENSP00000498629.1:n.-37-7548C=
ENST00000673637.1:c.-38+148C= ENSP00000501310.1:n.-38+148C=
ENST00000673922.1:n.235C=
ENST00000234420.9:c.146C= ENSP00000234420.4:p.Ala49=
ENST00000445503.5:c.146C= ENSP00000405294.1:p.Ala49=
ENST00000456246.1:c.146C= ENSP00000410570.1:p.Ala49=
ENST00000493177.1:n.210C=
ENST00000540021.5:c.146C= ENSP00000446475.1:p.Ala49=
ENST00000606499.1:c.-37-7548C= ENSP00000475605.1:n.-37-7548C=
ENST00000614496.4:c.-591C= ENSP00000477844.1:n.-591C=
ENST00000616033.4:c.144C= ENSP00000480261.1:p.Gly48=
ENST00000622629.4:c.-2951C= ENSP00000482078.1:n.-2951C=
NM_000179.2:c.146C= , LRG_219t1:c.146C= NP_000170.1:p.Ala49=
NM_001281492.1:c.146C= NP_001268421.1:p.Ala49=
NM_001281493.1:c.-591C= NP_001268422.1:n.-591C=
XM_011532800.1:c.-38+148C= XP_011531102.1:n.-38+148C=
XM_024452819.1:c.146C= XP_024308587.1:p.Ala49=
XM_024452822.1:c.-591C= XP_024308590.1:n.-591C=
NM_000179.3:c.146C= MANE Select NP_000170.1:p.Ala49=
NM_001281492.2:c.146C= NP_001268421.1:p.Ala49=
NM_001281493.2:c.-591C= NP_001268422.1:n.-591C=