Canonical Allele Identifier: CA2496038122

Gene: MSH6

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47783333_47783344delinsGCCGCCGCTGCC , CM000664.2:g.47783333_47783344delinsGCCGCCGCTGCC	GRCh38
NC_000002.11:g.48010472_48010483delinsGCCGCCGCTGCC , CM000664.1:g.48010472_48010483delinsGCCGCCGCTGCC	GRCh37
NC_000002.10:g.47863976_47863987delinsGCCGCCGCTGCC	NCBI36
NG_007111.1:g.5187_5198delinsGCCGCCGCTGCC , LRG_219:g.5187_5198delinsGCCGCCGCTGCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000700004.2:c.100_111delinsGCCGCCGCTGCC	ENSP00000514752.2:p.Ala34=
ENST00000699999.1:n.184_195delinsGCCGCCGCTGCC
ENST00000700000.1:c.100_111delinsGCCGCCGCTGCC	ENSP00000514749.1:p.Ala34=
ENST00000700001.1:n.172_183delinsGCCGCCGCTGCC
ENST00000700002.1:c.100_111delinsGCCGCCGCTGCC	ENSP00000514750.1:p.Ala34=
ENST00000700003.1:c.100_111delinsGCCGCCGCTGCC	ENSP00000514751.1:p.Ala34=
ENST00000234420.11:c.100_111delinsGCCGCCGCTGCC MANE Select	ENSP00000234420.5:p.Ala34=
ENST00000540021.6:c.100_111delinsGCCGCCGCTGCC	ENSP00000446475.1:p.Ala34=
ENST00000652107.1:c.-37-7594_-37-7583delinsGCCGCCGCTGCC	ENSP00000498629.1:n.-37-7594_-37-7583delinsGCCGCCGCTGCC
ENST00000673637.1:c.-38+102_-38+113delinsGCCGCCGCTGCC	ENSP00000501310.1:n.-38+102_-38+113delinsGCCGCCGCTGCC
ENST00000673922.1:n.189_200delinsGCCGCCGCTGCC
ENST00000234420.9:c.100_111delinsGCCGCCGCTGCC	ENSP00000234420.4:p.Ala34=
ENST00000445503.5:c.100_111delinsGCCGCCGCTGCC	ENSP00000405294.1:p.Ala34=
ENST00000456246.1:c.100_111delinsGCCGCCGCTGCC	ENSP00000410570.1:p.Ala34=
ENST00000493177.1:n.164_175delinsGCCGCCGCTGCC
ENST00000540021.5:c.100_111delinsGCCGCCGCTGCC	ENSP00000446475.1:p.Ala34=
ENST00000606499.1:c.-37-7594_-37-7583delinsGCCGCCGCTGCC	ENSP00000475605.1:n.-37-7594_-37-7583delinsGCCGCCGCTGCC
ENST00000614496.4:c.-637_-626delinsGCCGCCGCTGCC	ENSP00000477844.1:n.-637_-626delinsGCCGCCGCTGCC
ENST00000616033.4:c.100_109delinsGCCGCCGCTGCC
ENST00000622629.4:c.-2997_-2986delinsGCCGCCGCTGCC	ENSP00000482078.1:n.-2997_-2986delinsGCCGCCGCTGCC
NM_000179.2:c.100_111delinsGCCGCCGCTGCC , LRG_219t1:c.100_111delinsGCCGCCGCTGCC	NP_000170.1:p.Ala34=
NM_001281492.1:c.100_111delinsGCCGCCGCTGCC	NP_001268421.1:p.Ala34=
NM_001281493.1:c.-637_-626delinsGCCGCCGCTGCC	NP_001268422.1:n.-637_-626delinsGCCGCCGCTGCC
XM_011532800.1:c.-38+102_-38+113delinsGCCGCCGCTGCC	XP_011531102.1:n.-38+102_-38+113delinsGCCGCCGCTGCC
XM_024452819.1:c.100_111delinsGCCGCCGCTGCC	XP_024308587.1:p.Ala34=
XM_024452822.1:c.-637_-626delinsGCCGCCGCTGCC	XP_024308590.1:n.-637_-626delinsGCCGCCGCTGCC
NM_000179.3:c.100_111delinsGCCGCCGCTGCC MANE Select	NP_000170.1:p.Ala34=
NM_001281492.2:c.100_111delinsGCCGCCGCTGCC	NP_001268421.1:p.Ala34=
NM_001281493.2:c.-637_-626delinsGCCGCCGCTGCC	NP_001268422.1:n.-637_-626delinsGCCGCCGCTGCC