Canonical Allele Identifier: CA2496054273

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806558C= , CM000664.2:g.47806558C=	GRCh38
NC_000002.11:g.48033697C= , CM000664.1:g.48033697C=	GRCh37
NC_000002.10:g.47887201C=	NCBI36
NG_007111.1:g.28412C= , LRG_219:g.28412C=
NG_008397.1:g.104118G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3611C= (MSH6)	ENSP00000406248.2:p.Ala1204=
ENST00000420813.6:c.3611C= (MSH6)	ENSP00000390382.2:p.Ala1204=
ENST00000455383.6:c.3611C= (MSH6)	ENSP00000397484.2:p.Ala1204=
ENST00000700004.2:c.3524C= (MSH6)	ENSP00000514752.2:p.Ala1175=
ENST00000699999.1:n.4582C= (MSH6)
ENST00000700000.1:c.2342C= (MSH6)	ENSP00000514749.1:p.Ala781=
ENST00000700002.1:c.3914C= (MSH6)	ENSP00000514750.1:p.Ala1305=
ENST00000700003.1:c.1363C= (MSH6)	ENSP00000514751.1:n.1363C=
ENST00000700004.1:c.2681C= (MSH6)	ENSP00000514752.1:p.Ala894=
ENST00000700005.1:n.2759C= (MSH6)
ENST00000700006.1:n.5066C= (MSH6)
ENST00000700007.1:n.2503C= (MSH6)
ENST00000700008.1:n.2170C= (MSH6)
ENST00000700009.1:n.2572C= (MSH6)
ENST00000700010.1:n.1317C= (MSH6)
ENST00000700011.1:n.3202C= (MSH6)
ENST00000682451.1:n.4190G= (FBXO11)
ENST00000684712.1:n.4452G= (FBXO11)
ENST00000234420.11:c.3908C= (MSH6) MANE Select	ENSP00000234420.5:p.Ala1303=
ENST00000540021.6:c.3518C= (MSH6)	ENSP00000446475.1:p.Ala1173=
ENST00000652107.1:c.3611C= (MSH6)	ENSP00000498629.1:p.Ala1204=
ENST00000673637.1:c.3611C= (MSH6)	ENSP00000501310.1:p.Ala1204=
ENST00000234420.9:c.3908C= (MSH6)	ENSP00000234420.4:p.Ala1303=
ENST00000405808.5:c.169+1637G= (FBXO11)	ENSP00000385127.1:n.169+1637G=
ENST00000434234.5:c.*124+1436G= (FBXO11)	ENSP00000402692.1:n.*124+1436G=
ENST00000445503.5:c.*3255C= (MSH6)	ENSP00000405294.1:n.*3255C=
ENST00000538136.1:c.3002C= (MSH6)	ENSP00000438580.1:p.Ala1001=
ENST00000540021.5:c.3518C= (MSH6)	ENSP00000446475.1:p.Ala1173=
ENST00000614496.4:c.3002C= (MSH6)	ENSP00000477844.1:p.Ala1001=
ENST00000622629.4:c.809C= (MSH6)	ENSP00000482078.1:p.Ala270=
NM_000179.2:c.3908C= , LRG_219t1:c.3908C= (MSH6)	NP_000170.1:p.Ala1303=
NM_001281492.1:c.3518C= (MSH6)	NP_001268421.1:p.Ala1173=
NM_001281493.1:c.3002C= (MSH6)	NP_001268422.1:p.Ala1001=
NM_001281494.1:c.3002C= (MSH6)	NP_001268423.1:p.Ala1001=
XM_005264271.1:c.3611C= (MSH6)	XP_005264328.1:p.Ala1204=
XM_011532798.1:c.3725C= (MSH6)	XP_011531100.1:p.Ala1242=
XM_011532799.1:c.3611C= (MSH6)	XP_011531101.1:p.Ala1204=
XM_011532800.1:c.3611C= (MSH6)	XP_011531102.1:p.Ala1204=
XM_024452819.1:c.4001C= (MSH6)	XP_024308587.1:p.Ala1334=
XM_024452820.1:c.3818C= (MSH6)	XP_024308588.1:p.Ala1273=
XM_024452821.1:c.3704C= (MSH6)	XP_024308589.1:p.Ala1235=
XM_024452822.1:c.3095C= (MSH6)	XP_024308590.1:p.Ala1032=
NM_000179.3:c.3908C= (MSH6) MANE Select	NP_000170.1:p.Ala1303=
NM_001281492.2:c.3518C= (MSH6)	NP_001268421.1:p.Ala1173=
NM_001281493.2:c.3002C= (MSH6)	NP_001268422.1:p.Ala1001=
NM_001281494.2:c.3002C= (MSH6)	NP_001268423.1:p.Ala1001=