Canonical Allele Identifier: CA2496054152

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806497_47806498delinsAT , CM000664.2:g.47806497_47806498delinsAT	GRCh38
NC_000002.11:g.48033636_48033637delinsAT , CM000664.1:g.48033636_48033637delinsAT	GRCh37
NC_000002.10:g.47887140_47887141delinsAT	NCBI36
NG_007111.1:g.28351_28352delinsAT , LRG_219:g.28351_28352delinsAT
NG_008397.1:g.104178_104179delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3550_3551delinsAT (MSH6)	ENSP00000406248.2:p.Ile1184=
ENST00000420813.6:c.3550_3551delinsAT (MSH6)	ENSP00000390382.2:p.Ile1184=
ENST00000455383.6:c.3550_3551delinsAT (MSH6)	ENSP00000397484.2:p.Ile1184=
ENST00000700004.2:c.3463_3464delinsAT (MSH6)	ENSP00000514752.2:p.Ile1155=
ENST00000699999.1:n.4521_4522delinsAT (MSH6)
ENST00000700000.1:c.2281_2282delinsAT (MSH6)	ENSP00000514749.1:p.Ile761=
ENST00000700002.1:c.3853_3854delinsAT (MSH6)	ENSP00000514750.1:p.Ile1285=
ENST00000700003.1:c.1302_1303delinsAT (MSH6)	ENSP00000514751.1:n.1302_1303delinsAT
ENST00000700004.1:c.2620_2621delinsAT (MSH6)	ENSP00000514752.1:p.Ile874=
ENST00000700005.1:n.2698_2699delinsAT (MSH6)
ENST00000700006.1:n.5005_5006delinsAT (MSH6)
ENST00000700007.1:n.2442_2443delinsAT (MSH6)
ENST00000700008.1:n.2109_2110delinsAT (MSH6)
ENST00000700009.1:n.2511_2512delinsAT (MSH6)
ENST00000700010.1:n.1256_1257delinsAT (MSH6)
ENST00000700011.1:n.3141_3142delinsAT (MSH6)
ENST00000682451.1:n.4250_4251delinsAT (FBXO11)
ENST00000684712.1:n.4512_4513delinsAT (FBXO11)
ENST00000234420.11:c.3847_3848delinsAT (MSH6) MANE Select	ENSP00000234420.5:p.Ile1283=
ENST00000540021.6:c.3457_3458delinsAT (MSH6)	ENSP00000446475.1:p.Ile1153=
ENST00000652107.1:c.3550_3551delinsAT (MSH6)	ENSP00000498629.1:p.Ile1184=
ENST00000673637.1:c.3550_3551delinsAT (MSH6)	ENSP00000501310.1:p.Ile1184=
ENST00000234420.9:c.3847_3848delinsAT (MSH6)	ENSP00000234420.4:p.Ile1283=
ENST00000405808.5:c.169+1697_169+1698delinsAT (FBXO11)	ENSP00000385127.1:n.169+1697_169+1698delinsAT
ENST00000434234.5:c.*124+1496_*124+1497delinsAT (FBXO11)	ENSP00000402692.1:n.*124+1496_*124+1497delinsAT
ENST00000445503.5:c.*3194_*3195delinsAT (MSH6)	ENSP00000405294.1:n.*3194_*3195delinsAT
ENST00000538136.1:c.2941_2942delinsAT (MSH6)	ENSP00000438580.1:p.Ile981=
ENST00000540021.5:c.3457_3458delinsAT (MSH6)	ENSP00000446475.1:p.Ile1153=
ENST00000614496.4:c.2941_2942delinsAT (MSH6)	ENSP00000477844.1:p.Ile981=
ENST00000622629.4:c.748_749delinsAT (MSH6)	ENSP00000482078.1:p.Ile250=
NM_000179.2:c.3847_3848delinsAT , LRG_219t1:c.3847_3848delinsAT (MSH6)	NP_000170.1:p.Ile1283=
NM_001281492.1:c.3457_3458delinsAT (MSH6)	NP_001268421.1:p.Ile1153=
NM_001281493.1:c.2941_2942delinsAT (MSH6)	NP_001268422.1:p.Ile981=
NM_001281494.1:c.2941_2942delinsAT (MSH6)	NP_001268423.1:p.Ile981=
XM_005264271.1:c.3550_3551delinsAT (MSH6)	XP_005264328.1:p.Ile1184=
XM_011532798.1:c.3664_3665delinsAT (MSH6)	XP_011531100.1:p.Ile1222=
XM_011532799.1:c.3550_3551delinsAT (MSH6)	XP_011531101.1:p.Ile1184=
XM_011532800.1:c.3550_3551delinsAT (MSH6)	XP_011531102.1:p.Ile1184=
XM_024452819.1:c.3940_3941delinsAT (MSH6)	XP_024308587.1:p.Ile1314=
XM_024452820.1:c.3757_3758delinsAT (MSH6)	XP_024308588.1:p.Ile1253=
XM_024452821.1:c.3643_3644delinsAT (MSH6)	XP_024308589.1:p.Ile1215=
XM_024452822.1:c.3034_3035delinsAT (MSH6)	XP_024308590.1:p.Ile1012=
NM_000179.3:c.3847_3848delinsAT (MSH6) MANE Select	NP_000170.1:p.Ile1283=
NM_001281492.2:c.3457_3458delinsAT (MSH6)	NP_001268421.1:p.Ile1153=
NM_001281493.2:c.2941_2942delinsAT (MSH6)	NP_001268422.1:p.Ile981=
NM_001281494.2:c.2941_2942delinsAT (MSH6)	NP_001268423.1:p.Ile981=