Canonical Allele Identifier: CA2496049701

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47800615G= , CM000664.2:g.47800615G=	GRCh38
NC_000002.11:g.48027754G= , CM000664.1:g.48027754G=	GRCh37
NC_000002.10:g.47881258G=	NCBI36
NG_007111.1:g.22469G= , LRG_219:g.22469G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.2335G= (MSH6)	ENSP00000406248.2:p.Val779=
ENST00000420813.6:c.2335G= (MSH6)	ENSP00000390382.2:p.Val779=
ENST00000455383.6:c.2335G= (MSH6)	ENSP00000397484.2:p.Val779=
ENST00000700004.2:c.2632G= (MSH6)	ENSP00000514752.2:p.Val878=
ENST00000699999.1:n.2716G= (MSH6)
ENST00000700000.1:c.1606+1026G= (MSH6)	ENSP00000514749.1:n.1606+1026G=
ENST00000700002.1:c.2638G= (MSH6)	ENSP00000514750.1:p.Val880=
ENST00000700003.1:c.628-2805G= (MSH6)	ENSP00000514751.1:n.628-2805G=
ENST00000700004.1:c.1789G= (MSH6)	ENSP00000514752.1:p.Val597=
ENST00000234420.11:c.2632G= (MSH6) MANE Select	ENSP00000234420.5:p.Val878=
ENST00000540021.6:c.2242G= (MSH6)	ENSP00000446475.1:p.Val748=
ENST00000652107.1:c.2335G= (MSH6)	ENSP00000498629.1:p.Val779=
ENST00000673637.1:c.2335G= (MSH6)	ENSP00000501310.1:p.Val779=
ENST00000234420.9:c.2632G= (MSH6)	ENSP00000234420.4:p.Val878=
ENST00000405808.5:c.169+7580C= (FBXO11)	ENSP00000385127.1:n.169+7580C=
ENST00000434234.5:c.*124+7379C= (FBXO11)	ENSP00000402692.1:n.*124+7379C=
ENST00000445503.5:c.*1979G= (MSH6)	ENSP00000405294.1:n.*1979G=
ENST00000538136.1:c.1726G= (MSH6)	ENSP00000438580.1:p.Val576=
ENST00000540021.5:c.2242G= (MSH6)	ENSP00000446475.1:p.Val748=
ENST00000614496.4:c.1726G= (MSH6)	ENSP00000477844.1:p.Val576=
ENST00000616033.4:c.2629G= (MSH6)	ENSP00000480261.1:p.Val877=
ENST00000622629.4:c.-465G= (MSH6)	ENSP00000482078.1:n.-465G=
NM_000179.2:c.2632G= , LRG_219t1:c.2632G= (MSH6)	NP_000170.1:p.Val878=
NM_001281492.1:c.2242G= (MSH6)	NP_001268421.1:p.Val748=
NM_001281493.1:c.1726G= (MSH6)	NP_001268422.1:p.Val576=
NM_001281494.1:c.1726G= (MSH6)	NP_001268423.1:p.Val576=
XM_005264271.1:c.2335G= (MSH6)	XP_005264328.1:p.Val779=
XM_011532798.1:c.2449G= (MSH6)	XP_011531100.1:p.Val817=
XM_011532799.1:c.2335G= (MSH6)	XP_011531101.1:p.Val779=
XM_011532800.1:c.2335G= (MSH6)	XP_011531102.1:p.Val779=
XM_024452819.1:c.2632G= (MSH6)	XP_024308587.1:p.Val878=
XM_024452820.1:c.2449G= (MSH6)	XP_024308588.1:p.Val817=
XM_024452821.1:c.2335G= (MSH6)	XP_024308589.1:p.Val779=
XM_024452822.1:c.1726G= (MSH6)	XP_024308590.1:p.Val576=
NM_000179.3:c.2632G= (MSH6) MANE Select	NP_000170.1:p.Val878=
NM_001281492.2:c.2242G= (MSH6)	NP_001268421.1:p.Val748=
NM_001281493.2:c.1726G= (MSH6)	NP_001268422.1:p.Val576=
NM_001281494.2:c.1726G= (MSH6)	NP_001268423.1:p.Val576=