Canonical Allele Identifier: CA2496054340

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806618_47806626delinsTTGAGAAGA , CM000664.2:g.47806618_47806626delinsTTGAGAAGA	GRCh38
NC_000002.11:g.48033757_48033765delinsTTGAGAAGA , CM000664.1:g.48033757_48033765delinsTTGAGAAGA	GRCh37
NC_000002.10:g.47887261_47887269delinsTTGAGAAGA	NCBI36
NG_007111.1:g.28472_28480delinsTTGAGAAGA , LRG_219:g.28472_28480delinsTTGAGAAGA
NG_008397.1:g.104050_104058delinsTCTTCTCAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.3671_3679delinsTTGAGAAGA (MSH6)	ENSP00000406248.2:p.Phe1224=
ENST00000420813.6:c.3671_3679delinsTTGAGAAGA (MSH6)	ENSP00000390382.2:p.Phe1224=
ENST00000455383.6:c.3671_3679delinsTTGAGAAGA (MSH6)	ENSP00000397484.2:p.Phe1224=
ENST00000700004.2:c.3584_3592delinsTTGAGAAGA (MSH6)	ENSP00000514752.2:p.Phe1195=
ENST00000699999.1:n.4642_4650delinsTTGAGAAGA (MSH6)
ENST00000700000.1:c.2402_2410delinsTTGAGAAGA (MSH6)	ENSP00000514749.1:p.Phe801=
ENST00000700002.1:c.3974_3982delinsTTGAGAAGA (MSH6)	ENSP00000514750.1:p.Phe1325=
ENST00000700003.1:c.1423_1431delinsTTGAGAAGA (MSH6)	ENSP00000514751.1:n.1423_1431delinsTTGAGAAGA
ENST00000700004.1:c.2741_2749delinsTTGAGAAGA (MSH6)	ENSP00000514752.1:p.Phe914=
ENST00000700005.1:n.2819_2827delinsTTGAGAAGA (MSH6)
ENST00000700006.1:n.5126_5134delinsTTGAGAAGA (MSH6)
ENST00000700007.1:n.2563_2571delinsTTGAGAAGA (MSH6)
ENST00000700008.1:n.2230_2238delinsTTGAGAAGA (MSH6)
ENST00000700009.1:n.2632_2640delinsTTGAGAAGA (MSH6)
ENST00000700010.1:n.1377_1385delinsTTGAGAAGA (MSH6)
ENST00000700011.1:n.3262_3270delinsTTGAGAAGA (MSH6)
ENST00000682451.1:n.4122_4130delinsTCTTCTCAA (FBXO11)
ENST00000684712.1:n.4384_4392delinsTCTTCTCAA (FBXO11)
ENST00000234420.11:c.3968_3976delinsTTGAGAAGA (MSH6) MANE Select	ENSP00000234420.5:p.Phe1323=
ENST00000540021.6:c.3578_3586delinsTTGAGAAGA (MSH6)	ENSP00000446475.1:p.Phe1193=
ENST00000652107.1:c.3671_3679delinsTTGAGAAGA (MSH6)	ENSP00000498629.1:p.Phe1224=
ENST00000673637.1:c.3671_3679delinsTTGAGAAGA (MSH6)	ENSP00000501310.1:p.Phe1224=
ENST00000234420.9:c.3968_3976delinsTTGAGAAGA (MSH6)	ENSP00000234420.4:p.Phe1323=
ENST00000405808.5:c.169+1569_169+1577delinsTCTTCTCAA (FBXO11)	ENSP00000385127.1:n.169+1569_169+1577delinsTCTTCTCAA
ENST00000434234.5:c.*124+1368_*124+1376delinsTCTTCTCAA (FBXO11)	ENSP00000402692.1:n.*124+1368_*124+1376delinsTCTTCTCAA
ENST00000445503.5:c.*3315_*3323delinsTTGAGAAGA (MSH6)	ENSP00000405294.1:n.*3315_*3323delinsTTGAGAAGA
ENST00000538136.1:c.3062_3070delinsTTGAGAAGA (MSH6)	ENSP00000438580.1:p.Phe1021=
ENST00000540021.5:c.3578_3586delinsTTGAGAAGA (MSH6)	ENSP00000446475.1:p.Phe1193=
ENST00000614496.4:c.3062_3070delinsTTGAGAAGA (MSH6)	ENSP00000477844.1:p.Phe1021=
ENST00000622629.4:c.869_877delinsTTGAGAAGA (MSH6)	ENSP00000482078.1:p.Phe290=
NM_000179.2:c.3968_3976delinsTTGAGAAGA , LRG_219t1:c.3968_3976delinsTTGAGAAGA (MSH6)	NP_000170.1:p.Phe1323=
NM_001281492.1:c.3578_3586delinsTTGAGAAGA (MSH6)	NP_001268421.1:p.Phe1193=
NM_001281493.1:c.3062_3070delinsTTGAGAAGA (MSH6)	NP_001268422.1:p.Phe1021=
NM_001281494.1:c.3062_3070delinsTTGAGAAGA (MSH6)	NP_001268423.1:p.Phe1021=
XM_005264271.1:c.3671_3679delinsTTGAGAAGA (MSH6)	XP_005264328.1:p.Phe1224=
XM_011532798.1:c.3785_3793delinsTTGAGAAGA (MSH6)	XP_011531100.1:p.Phe1262=
XM_011532799.1:c.3671_3679delinsTTGAGAAGA (MSH6)	XP_011531101.1:p.Phe1224=
XM_011532800.1:c.3671_3679delinsTTGAGAAGA (MSH6)	XP_011531102.1:p.Phe1224=
XM_024452819.1:c.4061_4069delinsTTGAGAAGA (MSH6)	XP_024308587.1:p.Phe1354=
XM_024452820.1:c.3878_3886delinsTTGAGAAGA (MSH6)	XP_024308588.1:p.Phe1293=
XM_024452821.1:c.3764_3772delinsTTGAGAAGA (MSH6)	XP_024308589.1:p.Phe1255=
XM_024452822.1:c.3155_3163delinsTTGAGAAGA (MSH6)	XP_024308590.1:p.Phe1052=
NM_000179.3:c.3968_3976delinsTTGAGAAGA (MSH6) MANE Select	NP_000170.1:p.Phe1323=
NM_001281492.2:c.3578_3586delinsTTGAGAAGA (MSH6)	NP_001268421.1:p.Phe1193=
NM_001281493.2:c.3062_3070delinsTTGAGAAGA (MSH6)	NP_001268422.1:p.Phe1021=
NM_001281494.2:c.3062_3070delinsTTGAGAAGA (MSH6)	NP_001268423.1:p.Phe1021=