Canonical Allele Identifier: CA2580067004

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47803506_47803508del , CM000664.2:g.47803506_47803508del	GRCh38
NC_000002.11:g.48030645_48030647del , CM000664.1:g.48030645_48030647del	GRCh37
NC_000002.10:g.47884149_47884151del	NCBI36
NG_007111.1:g.25360_25362del , LRG_219:g.25360_25362del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.2962_2964del (MSH6)	ENSP00000406248.2:p.Pro988del
ENST00000420813.6:c.2962_2964del (MSH6)	ENSP00000390382.2:p.Pro988del
ENST00000455383.6:c.2962_2964del (MSH6)	ENSP00000397484.2:p.Pro988del
ENST00000700004.2:c.3173-2112_3173-2110del (MSH6)	ENSP00000514752.2:n.3173-2112_3173-2110del
ENST00000699999.1:n.3343_3345del (MSH6)
ENST00000700000.1:c.1693_1695del (MSH6)	ENSP00000514749.1:p.Pro565del
ENST00000700002.1:c.3265_3267del (MSH6)	ENSP00000514750.1:p.Pro1089del
ENST00000700003.1:c.714_716del (MSH6)	ENSP00000514751.1:n.714_716del
ENST00000700004.1:c.2330-2112_2330-2110del (MSH6)	ENSP00000514752.1:n.2330-2112_2330-2110del
ENST00000700005.1:n.2110_2112del (MSH6)
ENST00000700006.1:n.2107_2109del (MSH6)
ENST00000700007.1:n.1264_1266del (MSH6)
ENST00000700008.1:n.838_840del (MSH6)
ENST00000700009.1:n.837_839del (MSH6)
ENST00000700010.1:n.668_670del (MSH6)
ENST00000700011.1:n.739_741del (MSH6)
ENST00000234420.11:c.3259_3261del (MSH6) MANE Select	ENSP00000234420.5:p.Pro1087del
ENST00000540021.6:c.2869_2871del (MSH6)	ENSP00000446475.1:p.Pro957del
ENST00000652107.1:c.2962_2964del (MSH6)	ENSP00000498629.1:p.Pro988del
ENST00000673637.1:c.2962_2964del (MSH6)	ENSP00000501310.1:p.Pro988del
ENST00000234420.9:c.3259_3261del (MSH6)	ENSP00000234420.4:p.Pro1087del
ENST00000405808.5:c.169+4692_169+4694del (FBXO11)	ENSP00000385127.1:n.169+4692_169+4694del
ENST00000434234.5:c.*124+4491_*124+4493del (FBXO11)	ENSP00000402692.1:n.*124+4491_*124+4493del
ENST00000445503.5:c.*2606_*2608del (MSH6)	ENSP00000405294.1:n.*2606_*2608del
ENST00000538136.1:c.2353_2355del (MSH6)	ENSP00000438580.1:p.Pro785del
ENST00000540021.5:c.2869_2871del (MSH6)	ENSP00000446475.1:p.Pro957del
ENST00000614496.4:c.2353_2355del (MSH6)	ENSP00000477844.1:p.Pro785del
ENST00000622629.4:c.163_165del (MSH6)	ENSP00000482078.1:p.Pro55del
NM_000179.2:c.3259_3261del , LRG_219t1:c.3259_3261del (MSH6)	NP_000170.1:p.Pro1087del
NM_001281492.1:c.2869_2871del (MSH6)	NP_001268421.1:p.Pro957del
NM_001281493.1:c.2353_2355del (MSH6)	NP_001268422.1:p.Pro785del
NM_001281494.1:c.2353_2355del (MSH6)	NP_001268423.1:p.Pro785del
XM_005264271.1:c.2962_2964del (MSH6)	XP_005264328.1:p.Pro988del
XM_011532798.1:c.3076_3078del (MSH6)	XP_011531100.1:p.Pro1026del
XM_011532799.1:c.2962_2964del (MSH6)	XP_011531101.1:p.Pro988del
XM_011532800.1:c.2962_2964del (MSH6)	XP_011531102.1:p.Pro988del
XM_024452819.1:c.3259_3261del (MSH6)	XP_024308587.1:p.Pro1087del
XM_024452820.1:c.3076_3078del (MSH6)	XP_024308588.1:p.Pro1026del
XM_024452821.1:c.2962_2964del (MSH6)	XP_024308589.1:p.Pro988del
XM_024452822.1:c.2353_2355del (MSH6)	XP_024308590.1:p.Pro785del
NM_000179.3:c.3259_3261del (MSH6) MANE Select	NP_000170.1:p.Pro1087del
NM_001281492.2:c.2869_2871del (MSH6)	NP_001268421.1:p.Pro957del
NM_001281493.2:c.2353_2355del (MSH6)	NP_001268422.1:p.Pro785del
NM_001281494.2:c.2353_2355del (MSH6)	NP_001268423.1:p.Pro785del