Canonical Allele Identifier: CA2496054127

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806285_47806288delinsCATT , CM000664.2:g.47806285_47806288delinsCATT	GRCh38
NC_000002.11:g.48033424_48033427delinsCATT , CM000664.1:g.48033424_48033427delinsCATT	GRCh37
NC_000002.10:g.47886928_47886931delinsCATT	NCBI36
NG_007111.1:g.28139_28142delinsCATT , LRG_219:g.28139_28142delinsCATT
NG_008397.1:g.104388_104391delinsAATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3431_3434delinsCATT (MSH6)	ENSP00000406248.2:p.Thr1144=
ENST00000420813.6:c.3431_3434delinsCATT (MSH6)	ENSP00000390382.2:p.Thr1144=
ENST00000455383.6:c.3431_3434delinsCATT (MSH6)	ENSP00000397484.2:p.Thr1144=
ENST00000700004.2:c.3344_3347delinsCATT (MSH6)	ENSP00000514752.2:p.Thr1115=
ENST00000699999.1:n.4402_4405delinsCATT (MSH6)
ENST00000700000.1:c.2162_2165delinsCATT (MSH6)	ENSP00000514749.1:p.Thr721=
ENST00000700002.1:c.3734_3737delinsCATT (MSH6)	ENSP00000514750.1:p.Thr1245=
ENST00000700003.1:c.1183_1186delinsCATT (MSH6)	ENSP00000514751.1:n.1183_1186delinsCATT
ENST00000700004.1:c.2501_2504delinsCATT (MSH6)	ENSP00000514752.1:p.Thr834=
ENST00000700005.1:n.2579_2582delinsCATT (MSH6)
ENST00000700006.1:n.4886_4889delinsCATT (MSH6)
ENST00000700007.1:n.2323_2326delinsCATT (MSH6)
ENST00000700008.1:n.1897_1900delinsCATT (MSH6)
ENST00000700009.1:n.2392_2395delinsCATT (MSH6)
ENST00000700010.1:n.1137_1140delinsCATT (MSH6)
ENST00000700011.1:n.3022_3025delinsCATT (MSH6)
ENST00000682451.1:n.4460_4463delinsAATG (FBXO11)
ENST00000684712.1:n.4722_4725delinsAATG (FBXO11)
ENST00000234420.11:c.3728_3731delinsCATT (MSH6) MANE Select	ENSP00000234420.5:p.Thr1243=
ENST00000540021.6:c.3338_3341delinsCATT (MSH6)	ENSP00000446475.1:p.Thr1113=
ENST00000652107.1:c.3431_3434delinsCATT (MSH6)	ENSP00000498629.1:p.Thr1144=
ENST00000673637.1:c.3431_3434delinsCATT (MSH6)	ENSP00000501310.1:p.Thr1144=
ENST00000234420.9:c.3728_3731delinsCATT (MSH6)	ENSP00000234420.4:p.Thr1243=
ENST00000405808.5:c.169+1907_169+1910delinsAATG (FBXO11)	ENSP00000385127.1:n.169+1907_169+1910delinsAATG
ENST00000434234.5:c.*124+1706_*124+1709delinsAATG (FBXO11)	ENSP00000402692.1:n.*124+1706_*124+1709delinsAATG
ENST00000445503.5:c.*3075_*3078delinsCATT (MSH6)	ENSP00000405294.1:n.*3075_*3078delinsCATT
ENST00000538136.1:c.2822_2825delinsCATT (MSH6)	ENSP00000438580.1:p.Thr941=
ENST00000540021.5:c.3338_3341delinsCATT (MSH6)	ENSP00000446475.1:p.Thr1113=
ENST00000614496.4:c.2822_2825delinsCATT (MSH6)	ENSP00000477844.1:p.Thr941=
ENST00000622629.4:c.632_635delinsCATT (MSH6)	ENSP00000482078.1:p.Thr211=
NM_000179.2:c.3728_3731delinsCATT , LRG_219t1:c.3728_3731delinsCATT (MSH6)	NP_000170.1:p.Thr1243=
NM_001281492.1:c.3338_3341delinsCATT (MSH6)	NP_001268421.1:p.Thr1113=
NM_001281493.1:c.2822_2825delinsCATT (MSH6)	NP_001268422.1:p.Thr941=
NM_001281494.1:c.2822_2825delinsCATT (MSH6)	NP_001268423.1:p.Thr941=
XM_005264271.1:c.3431_3434delinsCATT (MSH6)	XP_005264328.1:p.Thr1144=
XM_011532798.1:c.3545_3548delinsCATT (MSH6)	XP_011531100.1:p.Thr1182=
XM_011532799.1:c.3431_3434delinsCATT (MSH6)	XP_011531101.1:p.Thr1144=
XM_011532800.1:c.3431_3434delinsCATT (MSH6)	XP_011531102.1:p.Thr1144=
XM_024452819.1:c.3728_3731delinsCATT (MSH6)	XP_024308587.1:p.Thr1243=
XM_024452820.1:c.3545_3548delinsCATT (MSH6)	XP_024308588.1:p.Thr1182=
XM_024452821.1:c.3431_3434delinsCATT (MSH6)	XP_024308589.1:p.Thr1144=
XM_024452822.1:c.2822_2825delinsCATT (MSH6)	XP_024308590.1:p.Thr941=
NM_000179.3:c.3728_3731delinsCATT (MSH6) MANE Select	NP_000170.1:p.Thr1243=
NM_001281492.2:c.3338_3341delinsCATT (MSH6)	NP_001268421.1:p.Thr1113=
NM_001281493.2:c.2822_2825delinsCATT (MSH6)	NP_001268422.1:p.Thr941=
NM_001281494.2:c.2822_2825delinsCATT (MSH6)	NP_001268423.1:p.Thr941=