Canonical Allele Identifier: CA2586964885

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806310_47806311insATTA , CM000664.2:g.47806310_47806311insATTA	GRCh38
NC_000002.11:g.48033449_48033450insATTA , CM000664.1:g.48033449_48033450insATTA	GRCh37
NC_000002.10:g.47886953_47886954insATTA	NCBI36
NG_007111.1:g.28164_28165insATTA , LRG_219:g.28164_28165insATTA
NG_008397.1:g.104366_104367insAATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3456_3457insATTA (MSH6)	ENSP00000406248.2:p.Leu1153IlefsTer24
ENST00000420813.6:c.3456_3457insATTA (MSH6)	ENSP00000390382.2:p.Leu1153IlefsTer24
ENST00000455383.6:c.3456_3457insATTA (MSH6)	ENSP00000397484.2:p.Leu1153IlefsTer24
ENST00000700004.2:c.3369_3370insATTA (MSH6)	ENSP00000514752.2:p.Leu1124IlefsTer24
ENST00000699999.1:n.4427_4428insATTA (MSH6)
ENST00000700000.1:c.2187_2188insATTA (MSH6)	ENSP00000514749.1:p.Leu730IlefsTer24
ENST00000700002.1:c.3759_3760insATTA (MSH6)	ENSP00000514750.1:p.Leu1254IlefsTer24
ENST00000700003.1:c.1208_1209insATTA (MSH6)	ENSP00000514751.1:n.1208_1209insATTA
ENST00000700004.1:c.2526_2527insATTA (MSH6)	ENSP00000514752.1:p.Leu843IlefsTer24
ENST00000700005.1:n.2604_2605insATTA (MSH6)
ENST00000700006.1:n.4911_4912insATTA (MSH6)
ENST00000700007.1:n.2348_2349insATTA (MSH6)
ENST00000700008.1:n.1922_1923insATTA (MSH6)
ENST00000700009.1:n.2417_2418insATTA (MSH6)
ENST00000700010.1:n.1162_1163insATTA (MSH6)
ENST00000700011.1:n.3047_3048insATTA (MSH6)
ENST00000682451.1:n.4438_4439insAATT (FBXO11)
ENST00000684712.1:n.4700_4701insAATT (FBXO11)
ENST00000234420.11:c.3753_3754insATTA (MSH6) MANE Select	ENSP00000234420.5:p.Leu1252IlefsTer24
ENST00000540021.6:c.3363_3364insATTA (MSH6)	ENSP00000446475.1:p.Leu1122IlefsTer24
ENST00000652107.1:c.3456_3457insATTA (MSH6)	ENSP00000498629.1:p.Leu1153IlefsTer24
ENST00000673637.1:c.3456_3457insATTA (MSH6)	ENSP00000501310.1:p.Leu1153IlefsTer24
ENST00000234420.9:c.3753_3754insATTA (MSH6)	ENSP00000234420.4:p.Leu1252IlefsTer24
ENST00000405808.5:c.169+1885_169+1886insAATT (FBXO11)	ENSP00000385127.1:n.169+1885_169+1886insAATT
ENST00000434234.5:c.*124+1684_*124+1685insAATT (FBXO11)	ENSP00000402692.1:n.*124+1684_*124+1685insAATT
ENST00000445503.5:c.*3100_*3101insATTA (MSH6)	ENSP00000405294.1:n.*3100_*3101insATTA
ENST00000538136.1:c.2847_2848insATTA (MSH6)	ENSP00000438580.1:p.Leu950IlefsTer24
ENST00000540021.5:c.3363_3364insATTA (MSH6)	ENSP00000446475.1:p.Leu1122IlefsTer24
ENST00000614496.4:c.2847_2848insATTA (MSH6)	ENSP00000477844.1:p.Leu950IlefsTer24
ENST00000622629.4:c.655_656insATTA (MSH6)	ENSP00000482078.1:p.Ile219AsnfsTer3
NM_000179.2:c.3753_3754insATTA , LRG_219t1:c.3753_3754insATTA (MSH6)	NP_000170.1:p.Leu1252IlefsTer24
NM_001281492.1:c.3363_3364insATTA (MSH6)	NP_001268421.1:p.Leu1122IlefsTer24
NM_001281493.1:c.2847_2848insATTA (MSH6)	NP_001268422.1:p.Leu950IlefsTer24
NM_001281494.1:c.2847_2848insATTA (MSH6)	NP_001268423.1:p.Leu950IlefsTer24
XM_005264271.1:c.3456_3457insATTA (MSH6)	XP_005264328.1:p.Leu1153IlefsTer24
XM_011532798.1:c.3570_3571insATTA (MSH6)	XP_011531100.1:p.Leu1191IlefsTer24
XM_011532799.1:c.3456_3457insATTA (MSH6)	XP_011531101.1:p.Leu1153IlefsTer24
XM_011532800.1:c.3456_3457insATTA (MSH6)	XP_011531102.1:p.Leu1153IlefsTer24
XM_024452819.1:c.3753_3754insATTA (MSH6)	XP_024308587.1:p.Leu1252IlefsTer31
XM_024452820.1:c.3570_3571insATTA (MSH6)	XP_024308588.1:p.Leu1191IlefsTer31
XM_024452821.1:c.3456_3457insATTA (MSH6)	XP_024308589.1:p.Leu1153IlefsTer31
XM_024452822.1:c.2847_2848insATTA (MSH6)	XP_024308590.1:p.Leu950IlefsTer31
NM_000179.3:c.3753_3754insATTA (MSH6) MANE Select	NP_000170.1:p.Leu1252IlefsTer24
NM_001281492.2:c.3363_3364insATTA (MSH6)	NP_001268421.1:p.Leu1122IlefsTer24
NM_001281493.2:c.2847_2848insATTA (MSH6)	NP_001268422.1:p.Leu950IlefsTer24
NM_001281494.2:c.2847_2848insATTA (MSH6)	NP_001268423.1:p.Leu950IlefsTer24