Canonical Allele Identifier: CA2597474347

Gene: MSH6 FBXO11

Linked Data

• gnomAD v3: 2-47805206-G-GTTTTTTTTT
• gnomAD v4: 2-47805206-G-GTTTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47805209_47805210insTTTTTTTTT , CM000664.2:g.47805209_47805210insTTTTTTTTT	GRCh38
NC_000002.11:g.48032348_48032349insTTTTTTTTT , CM000664.1:g.48032348_48032349insTTTTTTTTT	GRCh37
NC_000002.10:g.47885852_47885853insTTTTTTTTT	NCBI36
NG_007111.1:g.27063_27064insTTTTTTTTT , LRG_219:g.27063_27064insTTTTTTTTT
NG_008397.1:g.105469_105470insAAAAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3259+182_3259+183insTTTTTTTTT (MSH6)	ENSP00000406248.2:n.3259+182_3259+183insTTTTTTTTT
ENST00000420813.6:c.3259+182_3259+183insTTTTTTTTT (MSH6)	ENSP00000390382.2:n.3259+182_3259+183insTTTTTTTTT
ENST00000455383.6:c.3259+182_3259+183insTTTTTTTTT (MSH6)	ENSP00000397484.2:n.3259+182_3259+183insTTTTTTTTT
ENST00000700004.2:c.3173-409_3173-408insTTTTTTTTT (MSH6)	ENSP00000514752.2:n.3173-409_3173-408insTTTTTTTTT
ENST00000699999.1:n.3822_3823insTTTTTTTTT (MSH6)
ENST00000700000.1:c.1990+182_1990+183insTTTTTTTTT (MSH6)	ENSP00000514749.1:n.1990+182_1990+183insTTTTTTTTT
ENST00000700002.1:c.3562+182_3562+183insTTTTTTTTT (MSH6)	ENSP00000514750.1:n.3562+182_3562+183insTTTTTTTTT
ENST00000700003.1:c.1011+182_1011+183insTTTTTTTTT (MSH6)	ENSP00000514751.1:n.1011+182_1011+183insTTTTTTTTT
ENST00000700004.1:c.2330-409_2330-408insTTTTTTTTT (MSH6)	ENSP00000514752.1:n.2330-409_2330-408insTTTTTTTTT
ENST00000700005.1:n.2407+182_2407+183insTTTTTTTTT (MSH6)
ENST00000700006.1:n.3810_3811insTTTTTTTTT (MSH6)
ENST00000700007.1:n.1743_1744insTTTTTTTTT (MSH6)
ENST00000700008.1:n.1317_1318insTTTTTTTTT (MSH6)
ENST00000700009.1:n.1316_1317insTTTTTTTTT (MSH6)
ENST00000700010.1:n.965+182_965+183insTTTTTTTTT (MSH6)
ENST00000700011.1:n.2442_2443insTTTTTTTTT (MSH6)
ENST00000234420.11:c.3556+182_3556+183insTTTTTTTTT (MSH6) MANE Select	ENSP00000234420.5:n.3556+182_3556+183insTTTTTTTTT
ENST00000540021.6:c.3166+182_3166+183insTTTTTTTTT (MSH6)	ENSP00000446475.1:n.3166+182_3166+183insTTTTTTTTT
ENST00000652107.1:c.3259+182_3259+183insTTTTTTTTT (MSH6)	ENSP00000498629.1:n.3259+182_3259+183insTTTTTTTTT
ENST00000673637.1:c.3259+182_3259+183insTTTTTTTTT (MSH6)	ENSP00000501310.1:n.3259+182_3259+183insTTTTTTTTT
ENST00000234420.9:c.3556+182_3556+183insTTTTTTTTT (MSH6)	ENSP00000234420.4:n.3556+182_3556+183insTTTTTTTTT
ENST00000405808.5:c.169+2988_169+2989insAAAAAAAAA (FBXO11)	ENSP00000385127.1:n.169+2988_169+2989insAAAAAAAAA
ENST00000434234.5:c.*124+2787_*124+2788insAAAAAAAAA (FBXO11)	ENSP00000402692.1:n.*124+2787_*124+2788insAAAAAAAAA
ENST00000445503.5:c.*2903+182_*2903+183insTTTTTTTTT (MSH6)	ENSP00000405294.1:n.*2903+182_*2903+183insTTTTTTTTT
ENST00000538136.1:c.2650+182_2650+183insTTTTTTTTT (MSH6)	ENSP00000438580.1:n.2650+182_2650+183insTTTTTTTTT
ENST00000540021.5:c.3166+182_3166+183insTTTTTTTTT (MSH6)	ENSP00000446475.1:n.3166+182_3166+183insTTTTTTTTT
ENST00000614496.4:c.2650+182_2650+183insTTTTTTTTT (MSH6)	ENSP00000477844.1:n.2650+182_2650+183insTTTTTTTTT
ENST00000622629.4:c.460+182_460+183insTTTTTTTTT (MSH6)	ENSP00000482078.1:n.460+182_460+183insTTTTTTTTT
NM_000179.2:c.3556+182_3556+183insTTTTTTTTT , LRG_219t1:c.3556+182_3556+183insTTTTTTTTT (MSH6)	NP_000170.1:n.3556+182_3556+183insTTTTTTTTT
NM_001281492.1:c.3166+182_3166+183insTTTTTTTTT (MSH6)	NP_001268421.1:n.3166+182_3166+183insTTTTTTTTT
NM_001281493.1:c.2650+182_2650+183insTTTTTTTTT (MSH6)	NP_001268422.1:n.2650+182_2650+183insTTTTTTTTT
NM_001281494.1:c.2650+182_2650+183insTTTTTTTTT (MSH6)	NP_001268423.1:n.2650+182_2650+183insTTTTTTTTT
XM_005264271.1:c.3259+182_3259+183insTTTTTTTTT (MSH6)	XP_005264328.1:n.3259+182_3259+183insTTTTTTTTT
XM_011532798.1:c.3373+182_3373+183insTTTTTTTTT (MSH6)	XP_011531100.1:n.3373+182_3373+183insTTTTTTTTT
XM_011532799.1:c.3259+182_3259+183insTTTTTTTTT (MSH6)	XP_011531101.1:n.3259+182_3259+183insTTTTTTTTT
XM_011532800.1:c.3259+182_3259+183insTTTTTTTTT (MSH6)	XP_011531102.1:n.3259+182_3259+183insTTTTTTTTT
XM_024452819.1:c.3556+182_3556+183insTTTTTTTTT (MSH6)	XP_024308587.1:n.3556+182_3556+183insTTTTTTTTT
XM_024452820.1:c.3373+182_3373+183insTTTTTTTTT (MSH6)	XP_024308588.1:n.3373+182_3373+183insTTTTTTTTT
XM_024452821.1:c.3259+182_3259+183insTTTTTTTTT (MSH6)	XP_024308589.1:n.3259+182_3259+183insTTTTTTTTT
XM_024452822.1:c.2650+182_2650+183insTTTTTTTTT (MSH6)	XP_024308590.1:n.2650+182_2650+183insTTTTTTTTT
NM_000179.3:c.3556+182_3556+183insTTTTTTTTT (MSH6) MANE Select	NP_000170.1:n.3556+182_3556+183insTTTTTTTTT
NM_001281492.2:c.3166+182_3166+183insTTTTTTTTT (MSH6)	NP_001268421.1:n.3166+182_3166+183insTTTTTTTTT
NM_001281493.2:c.2650+182_2650+183insTTTTTTTTT (MSH6)	NP_001268422.1:n.2650+182_2650+183insTTTTTTTTT
NM_001281494.2:c.2650+182_2650+183insTTTTTTTTT (MSH6)	NP_001268423.1:n.2650+182_2650+183insTTTTTTTTT