Canonical Allele Identifier: CA2496053469

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47805627_47805629delinsCAT , CM000664.2:g.47805627_47805629delinsCAT	GRCh38
NC_000002.11:g.48032766_48032768delinsCAT , CM000664.1:g.48032766_48032768delinsCAT	GRCh37
NC_000002.10:g.47886270_47886272delinsCAT	NCBI36
NG_007111.1:g.27481_27483delinsCAT , LRG_219:g.27481_27483delinsCAT
NG_008397.1:g.105047_105049delinsATG

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.3269_3271delinsCAT (MSH6)	ENSP00000406248.2:p.Thr1090=
ENST00000420813.6:c.3269_3271delinsCAT (MSH6)	ENSP00000390382.2:p.Thr1090=
ENST00000455383.6:c.3269_3271delinsCAT (MSH6)	ENSP00000397484.2:p.Thr1090=
ENST00000700004.2:c.3182_3184delinsCAT (MSH6)	ENSP00000514752.2:p.Thr1061=
ENST00000699999.1:n.4240_4242delinsCAT (MSH6)
ENST00000700000.1:c.2000_2002delinsCAT (MSH6)	ENSP00000514749.1:p.Thr667=
ENST00000700002.1:c.3572_3574delinsCAT (MSH6)	ENSP00000514750.1:p.Thr1191=
ENST00000700003.1:c.1021_1023delinsCAT (MSH6)	ENSP00000514751.1:n.1021_1023delinsCAT
ENST00000700004.1:c.2339_2341delinsCAT (MSH6)	ENSP00000514752.1:p.Thr780=
ENST00000700005.1:n.2417_2419delinsCAT (MSH6)
ENST00000700006.1:n.4228_4230delinsCAT (MSH6)
ENST00000700007.1:n.2161_2163delinsCAT (MSH6)
ENST00000700008.1:n.1735_1737delinsCAT (MSH6)
ENST00000700009.1:n.1734_1736delinsCAT (MSH6)
ENST00000700010.1:n.975_977delinsCAT (MSH6)
ENST00000700011.1:n.2860_2862delinsCAT (MSH6)
ENST00000234420.11:c.3566_3568delinsCAT (MSH6) MANE Select	ENSP00000234420.5:p.Thr1189=
ENST00000540021.6:c.3176_3178delinsCAT (MSH6)	ENSP00000446475.1:p.Thr1059=
ENST00000652107.1:c.3269_3271delinsCAT (MSH6)	ENSP00000498629.1:p.Thr1090=
ENST00000673637.1:c.3269_3271delinsCAT (MSH6)	ENSP00000501310.1:p.Thr1090=
ENST00000234420.9:c.3566_3568delinsCAT (MSH6)	ENSP00000234420.4:p.Thr1189=
ENST00000405808.5:c.169+2566_169+2568delinsATG (FBXO11)	ENSP00000385127.1:n.169+2566_169+2568deli...
ENST00000434234.5:c.*124+2365_*124+2367delinsATG (FBXO11)	ENSP00000402692.1:n.*124+2365_*124+2367de...
ENST00000445503.5:c.*2913_*2915delinsCAT (MSH6)	ENSP00000405294.1:n.*2913_*2915delinsCAT
ENST00000538136.1:c.2660_2662delinsCAT (MSH6)	ENSP00000438580.1:p.Thr887=
ENST00000540021.5:c.3176_3178delinsCAT (MSH6)	ENSP00000446475.1:p.Thr1059=
ENST00000614496.4:c.2660_2662delinsCAT (MSH6)	ENSP00000477844.1:p.Thr887=
ENST00000622629.4:c.470_472delinsCAT (MSH6)	ENSP00000482078.1:p.Thr157=
NM_000179.2:c.3566_3568delinsCAT , LRG_219t1:c.3566_3568delinsCAT (MSH6)	NP_000170.1:p.Thr1189=
NM_001281492.1:c.3176_3178delinsCAT (MSH6)	NP_001268421.1:p.Thr1059=
NM_001281493.1:c.2660_2662delinsCAT (MSH6)	NP_001268422.1:p.Thr887=
NM_001281494.1:c.2660_2662delinsCAT (MSH6)	NP_001268423.1:p.Thr887=
XM_005264271.1:c.3269_3271delinsCAT (MSH6)	XP_005264328.1:p.Thr1090=
XM_011532798.1:c.3383_3385delinsCAT (MSH6)	XP_011531100.1:p.Thr1128=
XM_011532799.1:c.3269_3271delinsCAT (MSH6)	XP_011531101.1:p.Thr1090=
XM_011532800.1:c.3269_3271delinsCAT (MSH6)	XP_011531102.1:p.Thr1090=
XM_024452819.1:c.3566_3568delinsCAT (MSH6)	XP_024308587.1:p.Thr1189=
XM_024452820.1:c.3383_3385delinsCAT (MSH6)	XP_024308588.1:p.Thr1128=
XM_024452821.1:c.3269_3271delinsCAT (MSH6)	XP_024308589.1:p.Thr1090=
XM_024452822.1:c.2660_2662delinsCAT (MSH6)	XP_024308590.1:p.Thr887=
NM_000179.3:c.3566_3568delinsCAT (MSH6) MANE Select	NP_000170.1:p.Thr1189=
NM_001281492.2:c.3176_3178delinsCAT (MSH6)	NP_001268421.1:p.Thr1059=
NM_001281493.2:c.2660_2662delinsCAT (MSH6)	NP_001268422.1:p.Thr887=
NM_001281494.2:c.2660_2662delinsCAT (MSH6)	NP_001268423.1:p.Thr887=