Canonical Allele Identifier: CA769468277

Gene: MSH6 FBXO11

Linked Data

• dbSNP Id: rs1259312231
• MyVariant Identifiers: chr2:g.48033844_48033849del (hg19) ; chr2:g.47806705_47806710del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806707_47806712del , CM000664.2:g.47806707_47806712del	GRCh38
NC_000002.11:g.48033846_48033851del , CM000664.1:g.48033846_48033851del	GRCh37
NC_000002.10:g.47887350_47887355del	NCBI36
NG_007111.1:g.28561_28566del , LRG_219:g.28561_28566del
NG_008397.1:g.103966_103971del

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.3704+56_3704+61del (MSH6)	ENSP00000406248.2:n.3704+56_3704+61del
ENST00000420813.6:c.3704+56_3704+61del (MSH6)	ENSP00000390382.2:n.3704+56_3704+61del
ENST00000455383.6:c.3704+56_3704+61del (MSH6)	ENSP00000397484.2:n.3704+56_3704+61del
ENST00000700004.2:c.3617+56_3617+61del (MSH6)	ENSP00000514752.2:n.3617+56_3617+61del
ENST00000699999.1:n.4675+56_4675+61del (MSH6)
ENST00000700000.1:c.2435+56_2435+61del (MSH6)	ENSP00000514749.1:n.2435+56_2435+61del
ENST00000700002.1:c.4007+56_4007+61del (MSH6)	ENSP00000514750.1:n.4007+56_4007+61del
ENST00000700003.1:c.1456+56_1456+61del (MSH6)	ENSP00000514751.1:n.1456+56_1456+61del
ENST00000700004.1:c.2774+56_2774+61del (MSH6)	ENSP00000514752.1:n.2774+56_2774+61del
ENST00000700005.1:n.2908_2913del (MSH6)
ENST00000700006.1:n.5215_5220del (MSH6)
ENST00000700007.1:n.2596+56_2596+61del (MSH6)
ENST00000700008.1:n.2263+56_2263+61del (MSH6)
ENST00000700009.1:n.2665+56_2665+61del (MSH6)
ENST00000700010.1:n.1410+56_1410+61del (MSH6)
ENST00000700011.1:n.3295+56_3295+61del (MSH6)
ENST00000682451.1:n.4038_4043del (FBXO11)
ENST00000684712.1:n.4300_4305del (FBXO11)
ENST00000234420.11:c.4001+56_4001+61del (MSH6) MANE Select	ENSP00000234420.5:n.4001+56_4001+61del
ENST00000540021.6:c.3611+56_3611+61del (MSH6)	ENSP00000446475.1:n.3611+56_3611+61del
ENST00000652107.1:c.3704+56_3704+61del (MSH6)	ENSP00000498629.1:n.3704+56_3704+61del
ENST00000673637.1:c.3704+56_3704+61del (MSH6)	ENSP00000501310.1:n.3704+56_3704+61del
ENST00000234420.9:c.4001+56_4001+61del (MSH6)	ENSP00000234420.4:n.4001+56_4001+61del
ENST00000405808.5:c.169+1485_169+1490del (FBXO11)	ENSP00000385127.1:n.169+1485_169+1490del
ENST00000434234.5:c.*124+1284_*124+1289del (FBXO11)	ENSP00000402692.1:n.*124+1284_*124+1289del
ENST00000445503.5:c.*3348+56_*3348+61del (MSH6)	ENSP00000405294.1:n.*3348+56_*3348+61del
ENST00000538136.1:c.3095+56_3095+61del (MSH6)	ENSP00000438580.1:n.3095+56_3095+61del
ENST00000540021.5:c.3611+56_3611+61del (MSH6)	ENSP00000446475.1:n.3611+56_3611+61del
ENST00000614496.4:c.3095+56_3095+61del (MSH6)	ENSP00000477844.1:n.3095+56_3095+61del
ENST00000622629.4:c.902+56_902+61del (MSH6)	ENSP00000482078.1:n.902+56_902+61del
NM_000179.2:c.4001+56_4001+61del , LRG_219t1:c.4001+56_4001+61del (MSH6)	NP_000170.1:n.4001+56_4001+61del
NM_001281492.1:c.3611+56_3611+61del (MSH6)	NP_001268421.1:n.3611+56_3611+61del
NM_001281493.1:c.3095+56_3095+61del (MSH6)	NP_001268422.1:n.3095+56_3095+61del
NM_001281494.1:c.3095+56_3095+61del (MSH6)	NP_001268423.1:n.3095+56_3095+61del
XM_005264271.1:c.3704+56_3704+61del (MSH6)	XP_005264328.1:n.3704+56_3704+61del
XM_011532798.1:c.3818+56_3818+61del (MSH6)	XP_011531100.1:n.3818+56_3818+61del
XM_011532799.1:c.3704+56_3704+61del (MSH6)	XP_011531101.1:n.3704+56_3704+61del
XM_011532800.1:c.3704+56_3704+61del (MSH6)	XP_011531102.1:n.3704+56_3704+61del
XM_024452819.1:c.4094+56_4094+61del (MSH6)	XP_024308587.1:n.4094+56_4094+61del
XM_024452820.1:c.3911+56_3911+61del (MSH6)	XP_024308588.1:n.3911+56_3911+61del
XM_024452821.1:c.3797+56_3797+61del (MSH6)	XP_024308589.1:n.3797+56_3797+61del
XM_024452822.1:c.3188+56_3188+61del (MSH6)	XP_024308590.1:n.3188+56_3188+61del
NM_000179.3:c.4001+56_4001+61del (MSH6) MANE Select	NP_000170.1:n.4001+56_4001+61del
NM_001281492.2:c.3611+56_3611+61del (MSH6)	NP_001268421.1:n.3611+56_3611+61del
NM_001281493.2:c.3095+56_3095+61del (MSH6)	NP_001268422.1:n.3095+56_3095+61del
NM_001281494.2:c.3095+56_3095+61del (MSH6)	NP_001268423.1:n.3095+56_3095+61del