Canonical Allele Identifier: CA2658969140

Gene: MSH6 FBXO11

Linked Data

• gnomAD v4: 2-47806699-C-CCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806699_47806700insCT , CM000664.2:g.47806699_47806700insCT	GRCh38
NC_000002.11:g.48033838_48033839insCT , CM000664.1:g.48033838_48033839insCT	GRCh37
NC_000002.10:g.47887342_47887343insCT	NCBI36
NG_007111.1:g.28553_28554insCT , LRG_219:g.28553_28554insCT
NG_008397.1:g.103976_103977insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3704+48_3704+49insCT (MSH6)	ENSP00000406248.2:n.3704+48_3704+49insCT
ENST00000420813.6:c.3704+48_3704+49insCT (MSH6)	ENSP00000390382.2:n.3704+48_3704+49insCT
ENST00000455383.6:c.3704+48_3704+49insCT (MSH6)	ENSP00000397484.2:n.3704+48_3704+49insCT
ENST00000700004.2:c.3617+48_3617+49insCT (MSH6)	ENSP00000514752.2:n.3617+48_3617+49insCT
ENST00000699999.1:n.4675+48_4675+49insCT (MSH6)
ENST00000700000.1:c.2435+48_2435+49insCT (MSH6)	ENSP00000514749.1:n.2435+48_2435+49insCT
ENST00000700002.1:c.4007+48_4007+49insCT (MSH6)	ENSP00000514750.1:n.4007+48_4007+49insCT
ENST00000700003.1:c.1456+48_1456+49insCT (MSH6)	ENSP00000514751.1:n.1456+48_1456+49insCT
ENST00000700004.1:c.2774+48_2774+49insCT (MSH6)	ENSP00000514752.1:n.2774+48_2774+49insCT
ENST00000700005.1:n.2900_2901insCT (MSH6)
ENST00000700006.1:n.5207_5208insCT (MSH6)
ENST00000700007.1:n.2596+48_2596+49insCT (MSH6)
ENST00000700008.1:n.2263+48_2263+49insCT (MSH6)
ENST00000700009.1:n.2665+48_2665+49insCT (MSH6)
ENST00000700010.1:n.1410+48_1410+49insCT (MSH6)
ENST00000700011.1:n.3295+48_3295+49insCT (MSH6)
ENST00000682451.1:n.4048_4049insAG (FBXO11)
ENST00000684712.1:n.4310_4311insAG (FBXO11)
ENST00000234420.11:c.4001+48_4001+49insCT (MSH6) MANE Select	ENSP00000234420.5:n.4001+48_4001+49insCT
ENST00000540021.6:c.3611+48_3611+49insCT (MSH6)	ENSP00000446475.1:n.3611+48_3611+49insCT
ENST00000652107.1:c.3704+48_3704+49insCT (MSH6)	ENSP00000498629.1:n.3704+48_3704+49insCT
ENST00000673637.1:c.3704+48_3704+49insCT (MSH6)	ENSP00000501310.1:n.3704+48_3704+49insCT
ENST00000234420.9:c.4001+48_4001+49insCT (MSH6)	ENSP00000234420.4:n.4001+48_4001+49insCT
ENST00000405808.5:c.169+1495_169+1496insAG (FBXO11)	ENSP00000385127.1:n.169+1495_169+1496insAG
ENST00000434234.5:c.*124+1294_*124+1295insAG (FBXO11)	ENSP00000402692.1:n.*124+1294_*124+1295insAG
ENST00000445503.5:c.*3348+48_*3348+49insCT (MSH6)	ENSP00000405294.1:n.*3348+48_*3348+49insCT
ENST00000538136.1:c.3095+48_3095+49insCT (MSH6)	ENSP00000438580.1:n.3095+48_3095+49insCT
ENST00000540021.5:c.3611+48_3611+49insCT (MSH6)	ENSP00000446475.1:n.3611+48_3611+49insCT
ENST00000614496.4:c.3095+48_3095+49insCT (MSH6)	ENSP00000477844.1:n.3095+48_3095+49insCT
ENST00000622629.4:c.902+48_902+49insCT (MSH6)	ENSP00000482078.1:n.902+48_902+49insCT
NM_000179.2:c.4001+48_4001+49insCT , LRG_219t1:c.4001+48_4001+49insCT (MSH6)	NP_000170.1:n.4001+48_4001+49insCT
NM_001281492.1:c.3611+48_3611+49insCT (MSH6)	NP_001268421.1:n.3611+48_3611+49insCT
NM_001281493.1:c.3095+48_3095+49insCT (MSH6)	NP_001268422.1:n.3095+48_3095+49insCT
NM_001281494.1:c.3095+48_3095+49insCT (MSH6)	NP_001268423.1:n.3095+48_3095+49insCT
XM_005264271.1:c.3704+48_3704+49insCT (MSH6)	XP_005264328.1:n.3704+48_3704+49insCT
XM_011532798.1:c.3818+48_3818+49insCT (MSH6)	XP_011531100.1:n.3818+48_3818+49insCT
XM_011532799.1:c.3704+48_3704+49insCT (MSH6)	XP_011531101.1:n.3704+48_3704+49insCT
XM_011532800.1:c.3704+48_3704+49insCT (MSH6)	XP_011531102.1:n.3704+48_3704+49insCT
XM_024452819.1:c.4094+48_4094+49insCT (MSH6)	XP_024308587.1:n.4094+48_4094+49insCT
XM_024452820.1:c.3911+48_3911+49insCT (MSH6)	XP_024308588.1:n.3911+48_3911+49insCT
XM_024452821.1:c.3797+48_3797+49insCT (MSH6)	XP_024308589.1:n.3797+48_3797+49insCT
XM_024452822.1:c.3188+48_3188+49insCT (MSH6)	XP_024308590.1:n.3188+48_3188+49insCT
NM_000179.3:c.4001+48_4001+49insCT (MSH6) MANE Select	NP_000170.1:n.4001+48_4001+49insCT
NM_001281492.2:c.3611+48_3611+49insCT (MSH6)	NP_001268421.1:n.3611+48_3611+49insCT
NM_001281493.2:c.3095+48_3095+49insCT (MSH6)	NP_001268422.1:n.3095+48_3095+49insCT
NM_001281494.2:c.3095+48_3095+49insCT (MSH6)	NP_001268423.1:n.3095+48_3095+49insCT