Canonical Allele Identifier: CA2496038180

Gene: MSH6

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47783395_47783409delinsGCCTGGGCCCAGGCC , CM000664.2:g.47783395_47783409delinsGCCTGGGCCCAGGCC	GRCh38
NC_000002.11:g.48010534_48010548delinsGCCTGGGCCCAGGCC , CM000664.1:g.48010534_48010548delinsGCCTGGGCCCAGGCC	GRCh37
NC_000002.10:g.47864038_47864052delinsGCCTGGGCCCAGGCC	NCBI36
NG_007111.1:g.5249_5263delinsGCCTGGGCCCAGGCC , LRG_219:g.5249_5263delinsGCCTGGGCCCAGGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700004.2:c.162_176delinsGCCTGGGCCCAGGCC	ENSP00000514752.2:p.Gly54=
ENST00000699999.1:n.246_260delinsGCCTGGGCCCAGGCC
ENST00000700000.1:c.162_176delinsGCCTGGGCCCAGGCC	ENSP00000514749.1:p.Gly54=
ENST00000700001.1:n.234_248delinsGCCTGGGCCCAGGCC
ENST00000700002.1:c.162_176delinsGCCTGGGCCCAGGCC	ENSP00000514750.1:p.Gly54=
ENST00000700003.1:c.162_176delinsGCCTGGGCCCAGGCC	ENSP00000514751.1:p.Gly54=
ENST00000234420.11:c.162_176delinsGCCTGGGCCCAGGCC MANE Select	ENSP00000234420.5:p.Gly54=
ENST00000540021.6:c.162_176delinsGCCTGGGCCCAGGCC	ENSP00000446475.1:p.Gly54=
ENST00000652107.1:c.-37-7532_-37-7518delinsGCCTGGGCCCAGGCC	ENSP00000498629.1:n.-37-7532_-37-7518delinsGCCTGGGCCCAGGCC
ENST00000673637.1:c.-38+164_-38+178delinsGCCTGGGCCCAGGCC	ENSP00000501310.1:n.-38+164_-38+178delinsGCCTGGGCCCAGGCC
ENST00000673922.1:n.251_265delinsGCCTGGGCCCAGGCC
ENST00000234420.9:c.162_176delinsGCCTGGGCCCAGGCC	ENSP00000234420.4:p.Gly54=
ENST00000445503.5:c.162_176delinsGCCTGGGCCCAGGCC	ENSP00000405294.1:p.Gly54=
ENST00000456246.1:c.162_176delinsGCCTGGGCCCAGGCC	ENSP00000410570.1:p.Gly54=
ENST00000493177.1:n.226_240delinsGCCTGGGCCCAGGCC
ENST00000540021.5:c.162_176delinsGCCTGGGCCCAGGCC	ENSP00000446475.1:p.Gly54=
ENST00000606499.1:c.-37-7532_-37-7518delinsGCCTGGGCCCAGGCC	ENSP00000475605.1:n.-37-7532_-37-7518delinsGCCTGGGCCCAGGCC
ENST00000614496.4:c.-575_-561delinsGCCTGGGCCCAGGCC	ENSP00000477844.1:n.-575_-561delinsGCCTGGGCCCAGGCC
ENST00000616033.4:c.160_173delinsGCCTGGGCCCAGGCC
ENST00000622629.4:c.-2935_-2921delinsGCCTGGGCCCAGGCC	ENSP00000482078.1:n.-2935_-2921delinsGCCTGGGCCCAGGCC
NM_000179.2:c.162_176delinsGCCTGGGCCCAGGCC , LRG_219t1:c.162_176delinsGCCTGGGCCCAGGCC	NP_000170.1:p.Gly54=
NM_001281492.1:c.162_176delinsGCCTGGGCCCAGGCC	NP_001268421.1:p.Gly54=
NM_001281493.1:c.-575_-561delinsGCCTGGGCCCAGGCC	NP_001268422.1:n.-575_-561delinsGCCTGGGCCCAGGCC
XM_011532800.1:c.-38+164_-38+178delinsGCCTGGGCCCAGGCC	XP_011531102.1:n.-38+164_-38+178delinsGCCTGGGCCCAGGCC
XM_024452819.1:c.162_176delinsGCCTGGGCCCAGGCC	XP_024308587.1:p.Gly54=
XM_024452822.1:c.-575_-561delinsGCCTGGGCCCAGGCC	XP_024308590.1:n.-575_-561delinsGCCTGGGCCCAGGCC
NM_000179.3:c.162_176delinsGCCTGGGCCCAGGCC MANE Select	NP_000170.1:p.Gly54=
NM_001281492.2:c.162_176delinsGCCTGGGCCCAGGCC	NP_001268421.1:p.Gly54=
NM_001281493.2:c.-575_-561delinsGCCTGGGCCCAGGCC	NP_001268422.1:n.-575_-561delinsGCCTGGGCCCAGGCC