Canonical Allele Identifier: CA2825001141

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 3074415
• ClinVar RCV Id: RCV004013949

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806569_47806570insGAT , CM000664.2:g.47806569_47806570insGAT	GRCh38
NC_000002.11:g.48033708_48033709insGAT , CM000664.1:g.48033708_48033709insGAT	GRCh37
NC_000002.10:g.47887212_47887213insGAT	NCBI36
NG_007111.1:g.28423_28424insGAT , LRG_219:g.28423_28424insGAT
NG_008397.1:g.104106_104107insATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3622_3623insGAT (MSH6)	ENSP00000406248.2:p.Asn1208delinsArgTyr
ENST00000420813.6:c.3622_3623insGAT (MSH6)	ENSP00000390382.2:p.Asn1208delinsArgTyr
ENST00000455383.6:c.3622_3623insGAT (MSH6)	ENSP00000397484.2:p.Asn1208delinsArgTyr
ENST00000700004.2:c.3535_3536insGAT (MSH6)	ENSP00000514752.2:p.Asn1179delinsArgTyr
ENST00000699999.1:n.4593_4594insGAT (MSH6)
ENST00000700000.1:c.2353_2354insGAT (MSH6)	ENSP00000514749.1:p.Asn785delinsArgTyr
ENST00000700002.1:c.3925_3926insGAT (MSH6)	ENSP00000514750.1:p.Asn1309delinsArgTyr
ENST00000700003.1:c.1374_1375insGAT (MSH6)	ENSP00000514751.1:n.1374_1375insGAT
ENST00000700004.1:c.2692_2693insGAT (MSH6)	ENSP00000514752.1:p.Asn898delinsArgTyr
ENST00000700005.1:n.2770_2771insGAT (MSH6)
ENST00000700006.1:n.5077_5078insGAT (MSH6)
ENST00000700007.1:n.2514_2515insGAT (MSH6)
ENST00000700008.1:n.2181_2182insGAT (MSH6)
ENST00000700009.1:n.2583_2584insGAT (MSH6)
ENST00000700010.1:n.1328_1329insGAT (MSH6)
ENST00000700011.1:n.3213_3214insGAT (MSH6)
ENST00000682451.1:n.4178_4179insATC (FBXO11)
ENST00000684712.1:n.4440_4441insATC (FBXO11)
ENST00000234420.11:c.3919_3920insGAT (MSH6) MANE Select	ENSP00000234420.5:p.Asn1307delinsArgTyr
ENST00000540021.6:c.3529_3530insGAT (MSH6)	ENSP00000446475.1:p.Asn1177delinsArgTyr
ENST00000652107.1:c.3622_3623insGAT (MSH6)	ENSP00000498629.1:p.Asn1208delinsArgTyr
ENST00000673637.1:c.3622_3623insGAT (MSH6)	ENSP00000501310.1:p.Asn1208delinsArgTyr
ENST00000234420.9:c.3919_3920insGAT (MSH6)	ENSP00000234420.4:p.Asn1307delinsArgTyr
ENST00000405808.5:c.169+1625_169+1626insATC (FBXO11)	ENSP00000385127.1:n.169+1625_169+1626insATC
ENST00000434234.5:c.*124+1424_*124+1425insATC (FBXO11)	ENSP00000402692.1:n.*124+1424_*124+1425insATC
ENST00000445503.5:c.*3266_*3267insGAT (MSH6)	ENSP00000405294.1:n.*3266_*3267insGAT
ENST00000538136.1:c.3013_3014insGAT (MSH6)	ENSP00000438580.1:p.Asn1005delinsArgTyr
ENST00000540021.5:c.3529_3530insGAT (MSH6)	ENSP00000446475.1:p.Asn1177delinsArgTyr
ENST00000614496.4:c.3013_3014insGAT (MSH6)	ENSP00000477844.1:p.Asn1005delinsArgTyr
ENST00000622629.4:c.820_821insGAT (MSH6)	ENSP00000482078.1:p.Asn274delinsArgTyr
NM_000179.2:c.3919_3920insGAT , LRG_219t1:c.3919_3920insGAT (MSH6)	NP_000170.1:p.Asn1307delinsArgTyr
NM_001281492.1:c.3529_3530insGAT (MSH6)	NP_001268421.1:p.Asn1177delinsArgTyr
NM_001281493.1:c.3013_3014insGAT (MSH6)	NP_001268422.1:p.Asn1005delinsArgTyr
NM_001281494.1:c.3013_3014insGAT (MSH6)	NP_001268423.1:p.Asn1005delinsArgTyr
XM_005264271.1:c.3622_3623insGAT (MSH6)	XP_005264328.1:p.Asn1208delinsArgTyr
XM_011532798.1:c.3736_3737insGAT (MSH6)	XP_011531100.1:p.Asn1246delinsArgTyr
XM_011532799.1:c.3622_3623insGAT (MSH6)	XP_011531101.1:p.Asn1208delinsArgTyr
XM_011532800.1:c.3622_3623insGAT (MSH6)	XP_011531102.1:p.Asn1208delinsArgTyr
XM_024452819.1:c.4012_4013insGAT (MSH6)	XP_024308587.1:p.Asn1338delinsArgTyr
XM_024452820.1:c.3829_3830insGAT (MSH6)	XP_024308588.1:p.Asn1277delinsArgTyr
XM_024452821.1:c.3715_3716insGAT (MSH6)	XP_024308589.1:p.Asn1239delinsArgTyr
XM_024452822.1:c.3106_3107insGAT (MSH6)	XP_024308590.1:p.Asn1036delinsArgTyr
NM_000179.3:c.3919_3920insGAT (MSH6) MANE Select	NP_000170.1:p.Asn1307delinsArgTyr
NM_001281492.2:c.3529_3530insGAT (MSH6)	NP_001268421.1:p.Asn1177delinsArgTyr
NM_001281493.2:c.3013_3014insGAT (MSH6)	NP_001268422.1:p.Asn1005delinsArgTyr
NM_001281494.2:c.3013_3014insGAT (MSH6)	NP_001268423.1:p.Asn1005delinsArgTyr