Canonical Allele Identifier: CA2496054294

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806579_47806580delinsAG , CM000664.2:g.47806579_47806580delinsAG	GRCh38
NC_000002.11:g.48033718_48033719delinsAG , CM000664.1:g.48033718_48033719delinsAG	GRCh37
NC_000002.10:g.47887222_47887223delinsAG	NCBI36
NG_007111.1:g.28433_28434delinsAG , LRG_219:g.28433_28434delinsAG
NG_008397.1:g.104096_104097delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3632_3633delinsAG (MSH6)	ENSP00000406248.2:p.Glu1211=
ENST00000420813.6:c.3632_3633delinsAG (MSH6)	ENSP00000390382.2:p.Glu1211=
ENST00000455383.6:c.3632_3633delinsAG (MSH6)	ENSP00000397484.2:p.Glu1211=
ENST00000700004.2:c.3545_3546delinsAG (MSH6)	ENSP00000514752.2:p.Glu1182=
ENST00000699999.1:n.4603_4604delinsAG (MSH6)
ENST00000700000.1:c.2363_2364delinsAG (MSH6)	ENSP00000514749.1:p.Glu788=
ENST00000700002.1:c.3935_3936delinsAG (MSH6)	ENSP00000514750.1:p.Glu1312=
ENST00000700003.1:c.1384_1385delinsAG (MSH6)	ENSP00000514751.1:n.1384_1385delinsAG
ENST00000700004.1:c.2702_2703delinsAG (MSH6)	ENSP00000514752.1:p.Glu901=
ENST00000700005.1:n.2780_2781delinsAG (MSH6)
ENST00000700006.1:n.5087_5088delinsAG (MSH6)
ENST00000700007.1:n.2524_2525delinsAG (MSH6)
ENST00000700008.1:n.2191_2192delinsAG (MSH6)
ENST00000700009.1:n.2593_2594delinsAG (MSH6)
ENST00000700010.1:n.1338_1339delinsAG (MSH6)
ENST00000700011.1:n.3223_3224delinsAG (MSH6)
ENST00000682451.1:n.4168_4169delinsCT (FBXO11)
ENST00000684712.1:n.4430_4431delinsCT (FBXO11)
ENST00000234420.11:c.3929_3930delinsAG (MSH6) MANE Select	ENSP00000234420.5:p.Glu1310=
ENST00000540021.6:c.3539_3540delinsAG (MSH6)	ENSP00000446475.1:p.Glu1180=
ENST00000652107.1:c.3632_3633delinsAG (MSH6)	ENSP00000498629.1:p.Glu1211=
ENST00000673637.1:c.3632_3633delinsAG (MSH6)	ENSP00000501310.1:p.Glu1211=
ENST00000234420.9:c.3929_3930delinsAG (MSH6)	ENSP00000234420.4:p.Glu1310=
ENST00000405808.5:c.169+1615_169+1616delinsCT (FBXO11)	ENSP00000385127.1:n.169+1615_169+1616delinsCT
ENST00000434234.5:c.*124+1414_*124+1415delinsCT (FBXO11)	ENSP00000402692.1:n.*124+1414_*124+1415delinsCT
ENST00000445503.5:c.*3276_*3277delinsAG (MSH6)	ENSP00000405294.1:n.*3276_*3277delinsAG
ENST00000538136.1:c.3023_3024delinsAG (MSH6)	ENSP00000438580.1:p.Glu1008=
ENST00000540021.5:c.3539_3540delinsAG (MSH6)	ENSP00000446475.1:p.Glu1180=
ENST00000614496.4:c.3023_3024delinsAG (MSH6)	ENSP00000477844.1:p.Glu1008=
ENST00000622629.4:c.830_831delinsAG (MSH6)	ENSP00000482078.1:p.Glu277=
NM_000179.2:c.3929_3930delinsAG , LRG_219t1:c.3929_3930delinsAG (MSH6)	NP_000170.1:p.Glu1310=
NM_001281492.1:c.3539_3540delinsAG (MSH6)	NP_001268421.1:p.Glu1180=
NM_001281493.1:c.3023_3024delinsAG (MSH6)	NP_001268422.1:p.Glu1008=
NM_001281494.1:c.3023_3024delinsAG (MSH6)	NP_001268423.1:p.Glu1008=
XM_005264271.1:c.3632_3633delinsAG (MSH6)	XP_005264328.1:p.Glu1211=
XM_011532798.1:c.3746_3747delinsAG (MSH6)	XP_011531100.1:p.Glu1249=
XM_011532799.1:c.3632_3633delinsAG (MSH6)	XP_011531101.1:p.Glu1211=
XM_011532800.1:c.3632_3633delinsAG (MSH6)	XP_011531102.1:p.Glu1211=
XM_024452819.1:c.4022_4023delinsAG (MSH6)	XP_024308587.1:p.Glu1341=
XM_024452820.1:c.3839_3840delinsAG (MSH6)	XP_024308588.1:p.Glu1280=
XM_024452821.1:c.3725_3726delinsAG (MSH6)	XP_024308589.1:p.Glu1242=
XM_024452822.1:c.3116_3117delinsAG (MSH6)	XP_024308590.1:p.Glu1039=
NM_000179.3:c.3929_3930delinsAG (MSH6) MANE Select	NP_000170.1:p.Glu1310=
NM_001281492.2:c.3539_3540delinsAG (MSH6)	NP_001268421.1:p.Glu1180=
NM_001281493.2:c.3023_3024delinsAG (MSH6)	NP_001268422.1:p.Glu1008=
NM_001281494.2:c.3023_3024delinsAG (MSH6)	NP_001268423.1:p.Glu1008=