Canonical Allele Identifier: CA2496054067

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806457_47806471delinsCATGGTAGAAAATGA , CM000664.2:g.47806457_47806471delinsCATGGTAGAAAATGA	GRCh38
NC_000002.11:g.48033596_48033610delinsCATGGTAGAAAATGA , CM000664.1:g.48033596_48033610delinsCATGGTAGAAAATGA	GRCh37
NC_000002.10:g.47887100_47887114delinsCATGGTAGAAAATGA	NCBI36
NG_007111.1:g.28311_28325delinsCATGGTAGAAAATGA , LRG_219:g.28311_28325delinsCATGGTAGAAAATGA
NG_008397.1:g.104205_104219delinsTCATTTTCTACCATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3510_3524delinsCATGGTAGAAAATGA (MSH6)	ENSP00000406248.2:p.Cys1170=
ENST00000420813.6:c.3510_3524delinsCATGGTAGAAAATGA (MSH6)	ENSP00000390382.2:p.Cys1170=
ENST00000455383.6:c.3510_3524delinsCATGGTAGAAAATGA (MSH6)	ENSP00000397484.2:p.Cys1170=
ENST00000700004.2:c.3423_3437delinsCATGGTAGAAAATGA (MSH6)	ENSP00000514752.2:p.Cys1141=
ENST00000699999.1:n.4481_4495delinsCATGGTAGAAAATGA (MSH6)
ENST00000700000.1:c.2241_2255delinsCATGGTAGAAAATGA (MSH6)	ENSP00000514749.1:p.Cys747=
ENST00000700002.1:c.3813_3827delinsCATGGTAGAAAATGA (MSH6)	ENSP00000514750.1:p.Cys1271=
ENST00000700003.1:c.1262_1276delinsCATGGTAGAAAATGA (MSH6)	ENSP00000514751.1:n.1262_1276delinsCATGGTAGAAAATGA
ENST00000700004.1:c.2580_2594delinsCATGGTAGAAAATGA (MSH6)	ENSP00000514752.1:p.Cys860=
ENST00000700005.1:n.2658_2672delinsCATGGTAGAAAATGA (MSH6)
ENST00000700006.1:n.4965_4979delinsCATGGTAGAAAATGA (MSH6)
ENST00000700007.1:n.2402_2416delinsCATGGTAGAAAATGA (MSH6)
ENST00000700008.1:n.2069_2083delinsCATGGTAGAAAATGA (MSH6)
ENST00000700009.1:n.2471_2485delinsCATGGTAGAAAATGA (MSH6)
ENST00000700010.1:n.1216_1230delinsCATGGTAGAAAATGA (MSH6)
ENST00000700011.1:n.3101_3115delinsCATGGTAGAAAATGA (MSH6)
ENST00000682451.1:n.4277_4291delinsTCATTTTCTACCATG (FBXO11)
ENST00000684712.1:n.4539_4553delinsTCATTTTCTACCATG (FBXO11)
ENST00000234420.11:c.3807_3821delinsCATGGTAGAAAATGA (MSH6) MANE Select	ENSP00000234420.5:p.Cys1269=
ENST00000540021.6:c.3417_3431delinsCATGGTAGAAAATGA (MSH6)	ENSP00000446475.1:p.Cys1139=
ENST00000652107.1:c.3510_3524delinsCATGGTAGAAAATGA (MSH6)	ENSP00000498629.1:p.Cys1170=
ENST00000673637.1:c.3510_3524delinsCATGGTAGAAAATGA (MSH6)	ENSP00000501310.1:p.Cys1170=
ENST00000234420.9:c.3807_3821delinsCATGGTAGAAAATGA (MSH6)	ENSP00000234420.4:p.Cys1269=
ENST00000405808.5:c.169+1724_169+1738delinsTCATTTTCTACCATG (FBXO11)	ENSP00000385127.1:n.169+1724_169+1738delinsTCATTTTCTACCATG
ENST00000434234.5:c.*124+1523_*124+1537delinsTCATTTTCTACCATG (FBXO11)	ENSP00000402692.1:n.*124+1523_*124+1537delinsTCATTTTCTACCATG
ENST00000445503.5:c.*3154_*3168delinsCATGGTAGAAAATGA (MSH6)	ENSP00000405294.1:n.*3154_*3168delinsCATGGTAGAAAATGA
ENST00000538136.1:c.2901_2915delinsCATGGTAGAAAATGA (MSH6)	ENSP00000438580.1:p.Cys967=
ENST00000540021.5:c.3417_3431delinsCATGGTAGAAAATGA (MSH6)	ENSP00000446475.1:p.Cys1139=
ENST00000614496.4:c.2901_2915delinsCATGGTAGAAAATGA (MSH6)	ENSP00000477844.1:p.Cys967=
ENST00000622629.4:c.708_722delinsCATGGTAGAAAATGA (MSH6)	ENSP00000482078.1:p.Cys236=
NM_000179.2:c.3807_3821delinsCATGGTAGAAAATGA , LRG_219t1:c.3807_3821delinsCATGGTAGAAAATGA (MSH6)	NP_000170.1:p.Cys1269=
NM_001281492.1:c.3417_3431delinsCATGGTAGAAAATGA (MSH6)	NP_001268421.1:p.Cys1139=
NM_001281493.1:c.2901_2915delinsCATGGTAGAAAATGA (MSH6)	NP_001268422.1:p.Cys967=
NM_001281494.1:c.2901_2915delinsCATGGTAGAAAATGA (MSH6)	NP_001268423.1:p.Cys967=
XM_005264271.1:c.3510_3524delinsCATGGTAGAAAATGA (MSH6)	XP_005264328.1:p.Cys1170=
XM_011532798.1:c.3624_3638delinsCATGGTAGAAAATGA (MSH6)	XP_011531100.1:p.Cys1208=
XM_011532799.1:c.3510_3524delinsCATGGTAGAAAATGA (MSH6)	XP_011531101.1:p.Cys1170=
XM_011532800.1:c.3510_3524delinsCATGGTAGAAAATGA (MSH6)	XP_011531102.1:p.Cys1170=
XM_024452819.1:c.3900_3914delinsCATGGTAGAAAATGA (MSH6)	XP_024308587.1:p.Cys1300=
XM_024452820.1:c.3717_3731delinsCATGGTAGAAAATGA (MSH6)	XP_024308588.1:p.Cys1239=
XM_024452821.1:c.3603_3617delinsCATGGTAGAAAATGA (MSH6)	XP_024308589.1:p.Cys1201=
XM_024452822.1:c.2994_3008delinsCATGGTAGAAAATGA (MSH6)	XP_024308590.1:p.Cys998=
NM_000179.3:c.3807_3821delinsCATGGTAGAAAATGA (MSH6) MANE Select	NP_000170.1:p.Cys1269=
NM_001281492.2:c.3417_3431delinsCATGGTAGAAAATGA (MSH6)	NP_001268421.1:p.Cys1139=
NM_001281493.2:c.2901_2915delinsCATGGTAGAAAATGA (MSH6)	NP_001268422.1:p.Cys967=
NM_001281494.2:c.2901_2915delinsCATGGTAGAAAATGA (MSH6)	NP_001268423.1:p.Cys967=