Canonical Allele Identifier: CA2496054410

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806683_47806687delinsAACTG , CM000664.2:g.47806683_47806687delinsAACTG	GRCh38
NC_000002.11:g.48033822_48033826delinsAACTG , CM000664.1:g.48033822_48033826delinsAACTG	GRCh37
NC_000002.10:g.47887326_47887330delinsAACTG	NCBI36
NG_007111.1:g.28537_28541delinsAACTG , LRG_219:g.28537_28541delinsAACTG
NG_008397.1:g.103989_103993delinsCAGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3704+32_3704+36delinsAACTG (MSH6)	ENSP00000406248.2:n.3704+32_3704+36delinsAACTG
ENST00000420813.6:c.3704+32_3704+36delinsAACTG (MSH6)	ENSP00000390382.2:n.3704+32_3704+36delinsAACTG
ENST00000455383.6:c.3704+32_3704+36delinsAACTG (MSH6)	ENSP00000397484.2:n.3704+32_3704+36delinsAACTG
ENST00000700004.2:c.3617+32_3617+36delinsAACTG (MSH6)	ENSP00000514752.2:n.3617+32_3617+36delinsAACTG
ENST00000699999.1:n.4675+32_4675+36delinsAACTG (MSH6)
ENST00000700000.1:c.2435+32_2435+36delinsAACTG (MSH6)	ENSP00000514749.1:n.2435+32_2435+36delinsAACTG
ENST00000700002.1:c.4007+32_4007+36delinsAACTG (MSH6)	ENSP00000514750.1:n.4007+32_4007+36delinsAACTG
ENST00000700003.1:c.1456+32_1456+36delinsAACTG (MSH6)	ENSP00000514751.1:n.1456+32_1456+36delinsAACTG
ENST00000700004.1:c.2774+32_2774+36delinsAACTG (MSH6)	ENSP00000514752.1:n.2774+32_2774+36delinsAACTG
ENST00000700005.1:n.2884_2888delinsAACTG (MSH6)
ENST00000700006.1:n.5191_5195delinsAACTG (MSH6)
ENST00000700007.1:n.2596+32_2596+36delinsAACTG (MSH6)
ENST00000700008.1:n.2263+32_2263+36delinsAACTG (MSH6)
ENST00000700009.1:n.2665+32_2665+36delinsAACTG (MSH6)
ENST00000700010.1:n.1410+32_1410+36delinsAACTG (MSH6)
ENST00000700011.1:n.3295+32_3295+36delinsAACTG (MSH6)
ENST00000682451.1:n.4061_4065delinsCAGTT (FBXO11)
ENST00000684712.1:n.4323_4327delinsCAGTT (FBXO11)
ENST00000234420.11:c.4001+32_4001+36delinsAACTG (MSH6) MANE Select	ENSP00000234420.5:n.4001+32_4001+36delinsAACTG
ENST00000540021.6:c.3611+32_3611+36delinsAACTG (MSH6)	ENSP00000446475.1:n.3611+32_3611+36delinsAACTG
ENST00000652107.1:c.3704+32_3704+36delinsAACTG (MSH6)	ENSP00000498629.1:n.3704+32_3704+36delinsAACTG
ENST00000673637.1:c.3704+32_3704+36delinsAACTG (MSH6)	ENSP00000501310.1:n.3704+32_3704+36delinsAACTG
ENST00000234420.9:c.4001+32_4001+36delinsAACTG (MSH6)	ENSP00000234420.4:n.4001+32_4001+36delinsAACTG
ENST00000405808.5:c.169+1508_169+1512delinsCAGTT (FBXO11)	ENSP00000385127.1:n.169+1508_169+1512delinsCAGTT
ENST00000434234.5:c.*124+1307_*124+1311delinsCAGTT (FBXO11)	ENSP00000402692.1:n.*124+1307_*124+1311delinsCAGTT
ENST00000445503.5:c.*3348+32_*3348+36delinsAACTG (MSH6)	ENSP00000405294.1:n.*3348+32_*3348+36delinsAACTG
ENST00000538136.1:c.3095+32_3095+36delinsAACTG (MSH6)	ENSP00000438580.1:n.3095+32_3095+36delinsAACTG
ENST00000540021.5:c.3611+32_3611+36delinsAACTG (MSH6)	ENSP00000446475.1:n.3611+32_3611+36delinsAACTG
ENST00000614496.4:c.3095+32_3095+36delinsAACTG (MSH6)	ENSP00000477844.1:n.3095+32_3095+36delinsAACTG
ENST00000622629.4:c.902+32_902+36delinsAACTG (MSH6)	ENSP00000482078.1:n.902+32_902+36delinsAACTG
NM_000179.2:c.4001+32_4001+36delinsAACTG , LRG_219t1:c.4001+32_4001+36delinsAACTG (MSH6)	NP_000170.1:n.4001+32_4001+36delinsAACTG
NM_001281492.1:c.3611+32_3611+36delinsAACTG (MSH6)	NP_001268421.1:n.3611+32_3611+36delinsAACTG
NM_001281493.1:c.3095+32_3095+36delinsAACTG (MSH6)	NP_001268422.1:n.3095+32_3095+36delinsAACTG
NM_001281494.1:c.3095+32_3095+36delinsAACTG (MSH6)	NP_001268423.1:n.3095+32_3095+36delinsAACTG
XM_005264271.1:c.3704+32_3704+36delinsAACTG (MSH6)	XP_005264328.1:n.3704+32_3704+36delinsAACTG
XM_011532798.1:c.3818+32_3818+36delinsAACTG (MSH6)	XP_011531100.1:n.3818+32_3818+36delinsAACTG
XM_011532799.1:c.3704+32_3704+36delinsAACTG (MSH6)	XP_011531101.1:n.3704+32_3704+36delinsAACTG
XM_011532800.1:c.3704+32_3704+36delinsAACTG (MSH6)	XP_011531102.1:n.3704+32_3704+36delinsAACTG
XM_024452819.1:c.4094+32_4094+36delinsAACTG (MSH6)	XP_024308587.1:n.4094+32_4094+36delinsAACTG
XM_024452820.1:c.3911+32_3911+36delinsAACTG (MSH6)	XP_024308588.1:n.3911+32_3911+36delinsAACTG
XM_024452821.1:c.3797+32_3797+36delinsAACTG (MSH6)	XP_024308589.1:n.3797+32_3797+36delinsAACTG
XM_024452822.1:c.3188+32_3188+36delinsAACTG (MSH6)	XP_024308590.1:n.3188+32_3188+36delinsAACTG
NM_000179.3:c.4001+32_4001+36delinsAACTG (MSH6) MANE Select	NP_000170.1:n.4001+32_4001+36delinsAACTG
NM_001281492.2:c.3611+32_3611+36delinsAACTG (MSH6)	NP_001268421.1:n.3611+32_3611+36delinsAACTG
NM_001281493.2:c.3095+32_3095+36delinsAACTG (MSH6)	NP_001268422.1:n.3095+32_3095+36delinsAACTG
NM_001281494.2:c.3095+32_3095+36delinsAACTG (MSH6)	NP_001268423.1:n.3095+32_3095+36delinsAACTG