Canonical Allele Identifier: CA2496054080

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806463_47806469delinsAGAAAAT , CM000664.2:g.47806463_47806469delinsAGAAAAT	GRCh38
NC_000002.11:g.48033602_48033608delinsAGAAAAT , CM000664.1:g.48033602_48033608delinsAGAAAAT	GRCh37
NC_000002.10:g.47887106_47887112delinsAGAAAAT	NCBI36
NG_007111.1:g.28317_28323delinsAGAAAAT , LRG_219:g.28317_28323delinsAGAAAAT
NG_008397.1:g.104207_104213delinsATTTTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3516_3522delinsAGAAAAT (MSH6)	ENSP00000406248.2:p.Val1172=
ENST00000420813.6:c.3516_3522delinsAGAAAAT (MSH6)	ENSP00000390382.2:p.Val1172=
ENST00000455383.6:c.3516_3522delinsAGAAAAT (MSH6)	ENSP00000397484.2:p.Val1172=
ENST00000700004.2:c.3429_3435delinsAGAAAAT (MSH6)	ENSP00000514752.2:p.Val1143=
ENST00000699999.1:n.4487_4493delinsAGAAAAT (MSH6)
ENST00000700000.1:c.2247_2253delinsAGAAAAT (MSH6)	ENSP00000514749.1:p.Val749=
ENST00000700002.1:c.3819_3825delinsAGAAAAT (MSH6)	ENSP00000514750.1:p.Val1273=
ENST00000700003.1:c.1268_1274delinsAGAAAAT (MSH6)	ENSP00000514751.1:n.1268_1274delinsAGAAAAT
ENST00000700004.1:c.2586_2592delinsAGAAAAT (MSH6)	ENSP00000514752.1:p.Val862=
ENST00000700005.1:n.2664_2670delinsAGAAAAT (MSH6)
ENST00000700006.1:n.4971_4977delinsAGAAAAT (MSH6)
ENST00000700007.1:n.2408_2414delinsAGAAAAT (MSH6)
ENST00000700008.1:n.2075_2081delinsAGAAAAT (MSH6)
ENST00000700009.1:n.2477_2483delinsAGAAAAT (MSH6)
ENST00000700010.1:n.1222_1228delinsAGAAAAT (MSH6)
ENST00000700011.1:n.3107_3113delinsAGAAAAT (MSH6)
ENST00000682451.1:n.4279_4285delinsATTTTCT (FBXO11)
ENST00000684712.1:n.4541_4547delinsATTTTCT (FBXO11)
ENST00000234420.11:c.3813_3819delinsAGAAAAT (MSH6) MANE Select	ENSP00000234420.5:p.Val1271=
ENST00000540021.6:c.3423_3429delinsAGAAAAT (MSH6)	ENSP00000446475.1:p.Val1141=
ENST00000652107.1:c.3516_3522delinsAGAAAAT (MSH6)	ENSP00000498629.1:p.Val1172=
ENST00000673637.1:c.3516_3522delinsAGAAAAT (MSH6)	ENSP00000501310.1:p.Val1172=
ENST00000234420.9:c.3813_3819delinsAGAAAAT (MSH6)	ENSP00000234420.4:p.Val1271=
ENST00000405808.5:c.169+1726_169+1732delinsATTTTCT (FBXO11)	ENSP00000385127.1:n.169+1726_169+1732delinsATTTTCT
ENST00000434234.5:c.*124+1525_*124+1531delinsATTTTCT (FBXO11)	ENSP00000402692.1:n.*124+1525_*124+1531delinsATTTTCT
ENST00000445503.5:c.*3160_*3166delinsAGAAAAT (MSH6)	ENSP00000405294.1:n.*3160_*3166delinsAGAAAAT
ENST00000538136.1:c.2907_2913delinsAGAAAAT (MSH6)	ENSP00000438580.1:p.Val969=
ENST00000540021.5:c.3423_3429delinsAGAAAAT (MSH6)	ENSP00000446475.1:p.Val1141=
ENST00000614496.4:c.2907_2913delinsAGAAAAT (MSH6)	ENSP00000477844.1:p.Val969=
ENST00000622629.4:c.714_720delinsAGAAAAT (MSH6)	ENSP00000482078.1:p.Val238=
NM_000179.2:c.3813_3819delinsAGAAAAT , LRG_219t1:c.3813_3819delinsAGAAAAT (MSH6)	NP_000170.1:p.Val1271=
NM_001281492.1:c.3423_3429delinsAGAAAAT (MSH6)	NP_001268421.1:p.Val1141=
NM_001281493.1:c.2907_2913delinsAGAAAAT (MSH6)	NP_001268422.1:p.Val969=
NM_001281494.1:c.2907_2913delinsAGAAAAT (MSH6)	NP_001268423.1:p.Val969=
XM_005264271.1:c.3516_3522delinsAGAAAAT (MSH6)	XP_005264328.1:p.Val1172=
XM_011532798.1:c.3630_3636delinsAGAAAAT (MSH6)	XP_011531100.1:p.Val1210=
XM_011532799.1:c.3516_3522delinsAGAAAAT (MSH6)	XP_011531101.1:p.Val1172=
XM_011532800.1:c.3516_3522delinsAGAAAAT (MSH6)	XP_011531102.1:p.Val1172=
XM_024452819.1:c.3906_3912delinsAGAAAAT (MSH6)	XP_024308587.1:p.Val1302=
XM_024452820.1:c.3723_3729delinsAGAAAAT (MSH6)	XP_024308588.1:p.Val1241=
XM_024452821.1:c.3609_3615delinsAGAAAAT (MSH6)	XP_024308589.1:p.Val1203=
XM_024452822.1:c.3000_3006delinsAGAAAAT (MSH6)	XP_024308590.1:p.Val1000=
NM_000179.3:c.3813_3819delinsAGAAAAT (MSH6) MANE Select	NP_000170.1:p.Val1271=
NM_001281492.2:c.3423_3429delinsAGAAAAT (MSH6)	NP_001268421.1:p.Val1141=
NM_001281493.2:c.2907_2913delinsAGAAAAT (MSH6)	NP_001268422.1:p.Val969=
NM_001281494.2:c.2907_2913delinsAGAAAAT (MSH6)	NP_001268423.1:p.Val969=