Canonical Allele Identifier: CA2496038184

Gene: MSH6

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47783399_47783412delinsGGGCCCAGGCCCTT , CM000664.2:g.47783399_47783412delinsGGGCCCAGGCCCTT	GRCh38
NC_000002.11:g.48010538_48010551delinsGGGCCCAGGCCCTT , CM000664.1:g.48010538_48010551delinsGGGCCCAGGCCCTT	GRCh37
NC_000002.10:g.47864042_47864055delinsGGGCCCAGGCCCTT	NCBI36
NG_007111.1:g.5253_5266delinsGGGCCCAGGCCCTT , LRG_219:g.5253_5266delinsGGGCCCAGGCCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700004.2:c.166_179delinsGGGCCCAGGCCCTT	ENSP00000514752.2:p.Gly56=
ENST00000699999.1:n.250_263delinsGGGCCCAGGCCCTT
ENST00000700000.1:c.166_179delinsGGGCCCAGGCCCTT	ENSP00000514749.1:p.Gly56=
ENST00000700001.1:n.238_251delinsGGGCCCAGGCCCTT
ENST00000700002.1:c.166_179delinsGGGCCCAGGCCCTT	ENSP00000514750.1:p.Gly56=
ENST00000700003.1:c.166_179delinsGGGCCCAGGCCCTT	ENSP00000514751.1:p.Gly56=
ENST00000234420.11:c.166_179delinsGGGCCCAGGCCCTT MANE Select	ENSP00000234420.5:p.Gly56=
ENST00000540021.6:c.166_179delinsGGGCCCAGGCCCTT	ENSP00000446475.1:p.Gly56=
ENST00000652107.1:c.-37-7528_-37-7515delinsGGGCCCAGGCCCTT	ENSP00000498629.1:n.-37-7528_-37-7515delinsGGGCCCAGGCCCTT
ENST00000673637.1:c.-38+168_-38+181delinsGGGCCCAGGCCCTT	ENSP00000501310.1:n.-38+168_-38+181delinsGGGCCCAGGCCCTT
ENST00000673922.1:n.255_268delinsGGGCCCAGGCCCTT
ENST00000234420.9:c.166_179delinsGGGCCCAGGCCCTT	ENSP00000234420.4:p.Gly56=
ENST00000445503.5:c.166_179delinsGGGCCCAGGCCCTT	ENSP00000405294.1:p.Gly56=
ENST00000456246.1:c.166_179delinsGGGCCCAGGCCCTT	ENSP00000410570.1:p.Gly56=
ENST00000493177.1:n.230_243delinsGGGCCCAGGCCCTT
ENST00000540021.5:c.166_179delinsGGGCCCAGGCCCTT	ENSP00000446475.1:p.Gly56=
ENST00000606499.1:c.-37-7528_-37-7515delinsGGGCCCAGGCCCTT	ENSP00000475605.1:n.-37-7528_-37-7515delinsGGGCCCAGGCCCTT
ENST00000614496.4:c.-571_-558delinsGGGCCCAGGCCCTT	ENSP00000477844.1:n.-571_-558delinsGGGCCCAGGCCCTT
ENST00000616033.4:c.164_176delinsGGGCCCAGGCCCTT
ENST00000622629.4:c.-2931_-2918delinsGGGCCCAGGCCCTT	ENSP00000482078.1:n.-2931_-2918delinsGGGCCCAGGCCCTT
NM_000179.2:c.166_179delinsGGGCCCAGGCCCTT , LRG_219t1:c.166_179delinsGGGCCCAGGCCCTT	NP_000170.1:p.Gly56=
NM_001281492.1:c.166_179delinsGGGCCCAGGCCCTT	NP_001268421.1:p.Gly56=
NM_001281493.1:c.-571_-558delinsGGGCCCAGGCCCTT	NP_001268422.1:n.-571_-558delinsGGGCCCAGGCCCTT
XM_011532800.1:c.-38+168_-38+181delinsGGGCCCAGGCCCTT	XP_011531102.1:n.-38+168_-38+181delinsGGGCCCAGGCCCTT
XM_024452819.1:c.166_179delinsGGGCCCAGGCCCTT	XP_024308587.1:p.Gly56=
XM_024452822.1:c.-571_-558delinsGGGCCCAGGCCCTT	XP_024308590.1:n.-571_-558delinsGGGCCCAGGCCCTT
NM_000179.3:c.166_179delinsGGGCCCAGGCCCTT MANE Select	NP_000170.1:p.Gly56=
NM_001281492.2:c.166_179delinsGGGCCCAGGCCCTT	NP_001268421.1:p.Gly56=
NM_001281493.2:c.-571_-558delinsGGGCCCAGGCCCTT	NP_001268422.1:n.-571_-558delinsGGGCCCAGGCCCTT