Canonical Allele Identifier: CA2496038187

Gene: MSH6

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47783401_47783402delinsGC , CM000664.2:g.47783401_47783402delinsGC	GRCh38
NC_000002.11:g.48010540_48010541delinsGC , CM000664.1:g.48010540_48010541delinsGC	GRCh37
NC_000002.10:g.47864044_47864045delinsGC	NCBI36
NG_007111.1:g.5255_5256delinsGC , LRG_219:g.5255_5256delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700004.2:c.168_169delinsGC	ENSP00000514752.2:p.Gly56=
ENST00000699999.1:n.252_253delinsGC
ENST00000700000.1:c.168_169delinsGC	ENSP00000514749.1:p.Gly56=
ENST00000700001.1:n.240_241delinsGC
ENST00000700002.1:c.168_169delinsGC	ENSP00000514750.1:p.Gly56=
ENST00000700003.1:c.168_169delinsGC	ENSP00000514751.1:p.Gly56=
ENST00000234420.11:c.168_169delinsGC MANE Select	ENSP00000234420.5:p.Gly56=
ENST00000540021.6:c.168_169delinsGC	ENSP00000446475.1:p.Gly56=
ENST00000652107.1:c.-37-7526_-37-7525delinsGC	ENSP00000498629.1:n.-37-7526_-37-7525delinsGC
ENST00000673637.1:c.-38+170_-38+171delinsGC	ENSP00000501310.1:n.-38+170_-38+171delinsGC
ENST00000673922.1:n.257_258delinsGC
ENST00000234420.9:c.168_169delinsGC	ENSP00000234420.4:p.Gly56=
ENST00000445503.5:c.168_169delinsGC	ENSP00000405294.1:p.Gly56=
ENST00000456246.1:c.168_169delinsGC	ENSP00000410570.1:p.Gly56=
ENST00000493177.1:n.232_233delinsGC
ENST00000540021.5:c.168_169delinsGC	ENSP00000446475.1:p.Gly56=
ENST00000606499.1:c.-37-7526_-37-7525delinsGC	ENSP00000475605.1:n.-37-7526_-37-7525delinsGC
ENST00000614496.4:c.-569_-568delinsGC	ENSP00000477844.1:n.-569_-568delinsGC
ENST00000616033.4:c.166_167delinsGC	ENSP00000480261.1:p.Ala56=
ENST00000622629.4:c.-2929_-2928delinsGC	ENSP00000482078.1:n.-2929_-2928delinsGC
NM_000179.2:c.168_169delinsGC , LRG_219t1:c.168_169delinsGC	NP_000170.1:p.Gly56=
NM_001281492.1:c.168_169delinsGC	NP_001268421.1:p.Gly56=
NM_001281493.1:c.-569_-568delinsGC	NP_001268422.1:n.-569_-568delinsGC
XM_011532800.1:c.-38+170_-38+171delinsGC	XP_011531102.1:n.-38+170_-38+171delinsGC
XM_024452819.1:c.168_169delinsGC	XP_024308587.1:p.Gly56=
XM_024452822.1:c.-569_-568delinsGC	XP_024308590.1:n.-569_-568delinsGC
NM_000179.3:c.168_169delinsGC MANE Select	NP_000170.1:p.Gly56=
NM_001281492.2:c.168_169delinsGC	NP_001268421.1:p.Gly56=
NM_001281493.2:c.-569_-568delinsGC	NP_001268422.1:n.-569_-568delinsGC