Canonical Allele Identifier: CA2586964915

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806563_47806564insGCAA , CM000664.2:g.47806563_47806564insGCAA	GRCh38
NC_000002.11:g.48033702_48033703insGCAA , CM000664.1:g.48033702_48033703insGCAA	GRCh37
NC_000002.10:g.47887206_47887207insGCAA	NCBI36
NG_007111.1:g.28417_28418insGCAA , LRG_219:g.28417_28418insGCAA
NG_008397.1:g.104112_104113insTTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3616_3617insGCAA (MSH6)	ENSP00000406248.2:p.Leu1206ArgfsTer4
ENST00000420813.6:c.3616_3617insGCAA (MSH6)	ENSP00000390382.2:p.Leu1206ArgfsTer4
ENST00000455383.6:c.3616_3617insGCAA (MSH6)	ENSP00000397484.2:p.Leu1206ArgfsTer4
ENST00000700004.2:c.3529_3530insGCAA (MSH6)	ENSP00000514752.2:p.Leu1177ArgfsTer4
ENST00000699999.1:n.4587_4588insGCAA (MSH6)
ENST00000700000.1:c.2347_2348insGCAA (MSH6)	ENSP00000514749.1:p.Leu783ArgfsTer4
ENST00000700002.1:c.3919_3920insGCAA (MSH6)	ENSP00000514750.1:p.Leu1307ArgfsTer4
ENST00000700003.1:c.1368_1369insGCAA (MSH6)	ENSP00000514751.1:n.1368_1369insGCAA
ENST00000700004.1:c.2686_2687insGCAA (MSH6)	ENSP00000514752.1:p.Leu896ArgfsTer4
ENST00000700005.1:n.2764_2765insGCAA (MSH6)
ENST00000700006.1:n.5071_5072insGCAA (MSH6)
ENST00000700007.1:n.2508_2509insGCAA (MSH6)
ENST00000700008.1:n.2175_2176insGCAA (MSH6)
ENST00000700009.1:n.2577_2578insGCAA (MSH6)
ENST00000700010.1:n.1322_1323insGCAA (MSH6)
ENST00000700011.1:n.3207_3208insGCAA (MSH6)
ENST00000682451.1:n.4184_4185insTTGC (FBXO11)
ENST00000684712.1:n.4446_4447insTTGC (FBXO11)
ENST00000234420.11:c.3913_3914insGCAA (MSH6) MANE Select	ENSP00000234420.5:p.Leu1305ArgfsTer4
ENST00000540021.6:c.3523_3524insGCAA (MSH6)	ENSP00000446475.1:p.Leu1175ArgfsTer4
ENST00000652107.1:c.3616_3617insGCAA (MSH6)	ENSP00000498629.1:p.Leu1206ArgfsTer4
ENST00000673637.1:c.3616_3617insGCAA (MSH6)	ENSP00000501310.1:p.Leu1206ArgfsTer4
ENST00000234420.9:c.3913_3914insGCAA (MSH6)	ENSP00000234420.4:p.Leu1305ArgfsTer4
ENST00000405808.5:c.169+1631_169+1632insTTGC (FBXO11)	ENSP00000385127.1:n.169+1631_169+1632insTTGC
ENST00000434234.5:c.*124+1430_*124+1431insTTGC (FBXO11)	ENSP00000402692.1:n.*124+1430_*124+1431insTTGC
ENST00000445503.5:c.*3260_*3261insGCAA (MSH6)	ENSP00000405294.1:n.*3260_*3261insGCAA
ENST00000538136.1:c.3007_3008insGCAA (MSH6)	ENSP00000438580.1:p.Leu1003ArgfsTer4
ENST00000540021.5:c.3523_3524insGCAA (MSH6)	ENSP00000446475.1:p.Leu1175ArgfsTer4
ENST00000614496.4:c.3007_3008insGCAA (MSH6)	ENSP00000477844.1:p.Leu1003ArgfsTer4
ENST00000622629.4:c.814_815insGCAA (MSH6)	ENSP00000482078.1:p.Leu272ArgfsTer4
NM_000179.2:c.3913_3914insGCAA , LRG_219t1:c.3913_3914insGCAA (MSH6)	NP_000170.1:p.Leu1305ArgfsTer4
NM_001281492.1:c.3523_3524insGCAA (MSH6)	NP_001268421.1:p.Leu1175ArgfsTer4
NM_001281493.1:c.3007_3008insGCAA (MSH6)	NP_001268422.1:p.Leu1003ArgfsTer4
NM_001281494.1:c.3007_3008insGCAA (MSH6)	NP_001268423.1:p.Leu1003ArgfsTer4
XM_005264271.1:c.3616_3617insGCAA (MSH6)	XP_005264328.1:p.Leu1206ArgfsTer4
XM_011532798.1:c.3730_3731insGCAA (MSH6)	XP_011531100.1:p.Leu1244ArgfsTer4
XM_011532799.1:c.3616_3617insGCAA (MSH6)	XP_011531101.1:p.Leu1206ArgfsTer4
XM_011532800.1:c.3616_3617insGCAA (MSH6)	XP_011531102.1:p.Leu1206ArgfsTer4
XM_024452819.1:c.4006_4007insGCAA (MSH6)	XP_024308587.1:p.Leu1336ArgfsTer4
XM_024452820.1:c.3823_3824insGCAA (MSH6)	XP_024308588.1:p.Leu1275ArgfsTer4
XM_024452821.1:c.3709_3710insGCAA (MSH6)	XP_024308589.1:p.Leu1237ArgfsTer4
XM_024452822.1:c.3100_3101insGCAA (MSH6)	XP_024308590.1:p.Leu1034ArgfsTer4
NM_000179.3:c.3913_3914insGCAA (MSH6) MANE Select	NP_000170.1:p.Leu1305ArgfsTer4
NM_001281492.2:c.3523_3524insGCAA (MSH6)	NP_001268421.1:p.Leu1175ArgfsTer4
NM_001281493.2:c.3007_3008insGCAA (MSH6)	NP_001268422.1:p.Leu1003ArgfsTer4
NM_001281494.2:c.3007_3008insGCAA (MSH6)	NP_001268423.1:p.Leu1003ArgfsTer4