Canonical Allele Identifier: CA2496054147

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806496_47806501delinsTATTAC , CM000664.2:g.47806496_47806501delinsTATTAC	GRCh38
NC_000002.11:g.48033635_48033640delinsTATTAC , CM000664.1:g.48033635_48033640delinsTATTAC	GRCh37
NC_000002.10:g.47887139_47887144delinsTATTAC	NCBI36
NG_007111.1:g.28350_28355delinsTATTAC , LRG_219:g.28350_28355delinsTATTAC
NG_008397.1:g.104175_104180delinsGTAATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3549_3554delinsTATTAC (MSH6)	ENSP00000406248.2:p.Thr1183=
ENST00000420813.6:c.3549_3554delinsTATTAC (MSH6)	ENSP00000390382.2:p.Thr1183=
ENST00000455383.6:c.3549_3554delinsTATTAC (MSH6)	ENSP00000397484.2:p.Thr1183=
ENST00000700004.2:c.3462_3467delinsTATTAC (MSH6)	ENSP00000514752.2:p.Thr1154=
ENST00000699999.1:n.4520_4525delinsTATTAC (MSH6)
ENST00000700000.1:c.2280_2285delinsTATTAC (MSH6)	ENSP00000514749.1:p.Thr760=
ENST00000700002.1:c.3852_3857delinsTATTAC (MSH6)	ENSP00000514750.1:p.Thr1284=
ENST00000700003.1:c.1301_1306delinsTATTAC (MSH6)	ENSP00000514751.1:n.1301_1306delinsTATTAC
ENST00000700004.1:c.2619_2624delinsTATTAC (MSH6)	ENSP00000514752.1:p.Thr873=
ENST00000700005.1:n.2697_2702delinsTATTAC (MSH6)
ENST00000700006.1:n.5004_5009delinsTATTAC (MSH6)
ENST00000700007.1:n.2441_2446delinsTATTAC (MSH6)
ENST00000700008.1:n.2108_2113delinsTATTAC (MSH6)
ENST00000700009.1:n.2510_2515delinsTATTAC (MSH6)
ENST00000700010.1:n.1255_1260delinsTATTAC (MSH6)
ENST00000700011.1:n.3140_3145delinsTATTAC (MSH6)
ENST00000682451.1:n.4247_4252delinsGTAATA (FBXO11)
ENST00000684712.1:n.4509_4514delinsGTAATA (FBXO11)
ENST00000234420.11:c.3846_3851delinsTATTAC (MSH6) MANE Select	ENSP00000234420.5:p.Thr1282=
ENST00000540021.6:c.3456_3461delinsTATTAC (MSH6)	ENSP00000446475.1:p.Thr1152=
ENST00000652107.1:c.3549_3554delinsTATTAC (MSH6)	ENSP00000498629.1:p.Thr1183=
ENST00000673637.1:c.3549_3554delinsTATTAC (MSH6)	ENSP00000501310.1:p.Thr1183=
ENST00000234420.9:c.3846_3851delinsTATTAC (MSH6)	ENSP00000234420.4:p.Thr1282=
ENST00000405808.5:c.169+1694_169+1699delinsGTAATA (FBXO11)	ENSP00000385127.1:n.169+1694_169+1699delinsGTAATA
ENST00000434234.5:c.*124+1493_*124+1498delinsGTAATA (FBXO11)	ENSP00000402692.1:n.*124+1493_*124+1498delinsGTAATA
ENST00000445503.5:c.*3193_*3198delinsTATTAC (MSH6)	ENSP00000405294.1:n.*3193_*3198delinsTATTAC
ENST00000538136.1:c.2940_2945delinsTATTAC (MSH6)	ENSP00000438580.1:p.Thr980=
ENST00000540021.5:c.3456_3461delinsTATTAC (MSH6)	ENSP00000446475.1:p.Thr1152=
ENST00000614496.4:c.2940_2945delinsTATTAC (MSH6)	ENSP00000477844.1:p.Thr980=
ENST00000622629.4:c.747_752delinsTATTAC (MSH6)	ENSP00000482078.1:p.Thr249=
NM_000179.2:c.3846_3851delinsTATTAC , LRG_219t1:c.3846_3851delinsTATTAC (MSH6)	NP_000170.1:p.Thr1282=
NM_001281492.1:c.3456_3461delinsTATTAC (MSH6)	NP_001268421.1:p.Thr1152=
NM_001281493.1:c.2940_2945delinsTATTAC (MSH6)	NP_001268422.1:p.Thr980=
NM_001281494.1:c.2940_2945delinsTATTAC (MSH6)	NP_001268423.1:p.Thr980=
XM_005264271.1:c.3549_3554delinsTATTAC (MSH6)	XP_005264328.1:p.Thr1183=
XM_011532798.1:c.3663_3668delinsTATTAC (MSH6)	XP_011531100.1:p.Thr1221=
XM_011532799.1:c.3549_3554delinsTATTAC (MSH6)	XP_011531101.1:p.Thr1183=
XM_011532800.1:c.3549_3554delinsTATTAC (MSH6)	XP_011531102.1:p.Thr1183=
XM_024452819.1:c.3939_3944delinsTATTAC (MSH6)	XP_024308587.1:p.Thr1313=
XM_024452820.1:c.3756_3761delinsTATTAC (MSH6)	XP_024308588.1:p.Thr1252=
XM_024452821.1:c.3642_3647delinsTATTAC (MSH6)	XP_024308589.1:p.Thr1214=
XM_024452822.1:c.3033_3038delinsTATTAC (MSH6)	XP_024308590.1:p.Thr1011=
NM_000179.3:c.3846_3851delinsTATTAC (MSH6) MANE Select	NP_000170.1:p.Thr1282=
NM_001281492.2:c.3456_3461delinsTATTAC (MSH6)	NP_001268421.1:p.Thr1152=
NM_001281493.2:c.2940_2945delinsTATTAC (MSH6)	NP_001268422.1:p.Thr980=
NM_001281494.2:c.2940_2945delinsTATTAC (MSH6)	NP_001268423.1:p.Thr980=