Canonical Allele Identifier: CA2496054091

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806270_47806272delinsCTA , CM000664.2:g.47806270_47806272delinsCTA	GRCh38
NC_000002.11:g.48033409_48033411delinsCTA , CM000664.1:g.48033409_48033411delinsCTA	GRCh37
NC_000002.10:g.47886913_47886915delinsCTA	NCBI36
NG_007111.1:g.28124_28126delinsCTA , LRG_219:g.28124_28126delinsCTA
NG_008397.1:g.104404_104406delinsTAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.3416_3418delinsCTA (MSH6)	ENSP00000406248.2:p.Thr1139=
ENST00000420813.6:c.3416_3418delinsCTA (MSH6)	ENSP00000390382.2:p.Thr1139=
ENST00000455383.6:c.3416_3418delinsCTA (MSH6)	ENSP00000397484.2:p.Thr1139=
ENST00000700004.2:c.3329_3331delinsCTA (MSH6)	ENSP00000514752.2:p.Thr1110=
ENST00000699999.1:n.4387_4389delinsCTA (MSH6)
ENST00000700000.1:c.2147_2149delinsCTA (MSH6)	ENSP00000514749.1:p.Thr716=
ENST00000700002.1:c.3719_3721delinsCTA (MSH6)	ENSP00000514750.1:p.Thr1240=
ENST00000700003.1:c.1168_1170delinsCTA (MSH6)	ENSP00000514751.1:n.1168_1170delinsCTA
ENST00000700004.1:c.2486_2488delinsCTA (MSH6)	ENSP00000514752.1:p.Thr829=
ENST00000700005.1:n.2564_2566delinsCTA (MSH6)
ENST00000700006.1:n.4871_4873delinsCTA (MSH6)
ENST00000700007.1:n.2308_2310delinsCTA (MSH6)
ENST00000700008.1:n.1882_1884delinsCTA (MSH6)
ENST00000700009.1:n.2377_2379delinsCTA (MSH6)
ENST00000700010.1:n.1122_1124delinsCTA (MSH6)
ENST00000700011.1:n.3007_3009delinsCTA (MSH6)
ENST00000682451.1:n.4476_4478delinsTAG (FBXO11)
ENST00000684712.1:n.4738_4740delinsTAG (FBXO11)
ENST00000234420.11:c.3713_3715delinsCTA (MSH6) MANE Select	ENSP00000234420.5:p.Thr1238=
ENST00000540021.6:c.3323_3325delinsCTA (MSH6)	ENSP00000446475.1:p.Thr1108=
ENST00000652107.1:c.3416_3418delinsCTA (MSH6)	ENSP00000498629.1:p.Thr1139=
ENST00000673637.1:c.3416_3418delinsCTA (MSH6)	ENSP00000501310.1:p.Thr1139=
ENST00000234420.9:c.3713_3715delinsCTA (MSH6)	ENSP00000234420.4:p.Thr1238=
ENST00000405808.5:c.169+1923_169+1925delinsTAG (FBXO11)	ENSP00000385127.1:n.169+1923_169+1925deli...
ENST00000434234.5:c.*124+1722_*124+1724delinsTAG (FBXO11)	ENSP00000402692.1:n.*124+1722_*124+1724de...
ENST00000445503.5:c.*3060_*3062delinsCTA (MSH6)	ENSP00000405294.1:n.*3060_*3062delinsCTA
ENST00000538136.1:c.2807_2809delinsCTA (MSH6)	ENSP00000438580.1:p.Thr936=
ENST00000540021.5:c.3323_3325delinsCTA (MSH6)	ENSP00000446475.1:p.Thr1108=
ENST00000614496.4:c.2807_2809delinsCTA (MSH6)	ENSP00000477844.1:p.Thr936=
ENST00000622629.4:c.617_619delinsCTA (MSH6)	ENSP00000482078.1:p.Thr206=
NM_000179.2:c.3713_3715delinsCTA , LRG_219t1:c.3713_3715delinsCTA (MSH6)	NP_000170.1:p.Thr1238=
NM_001281492.1:c.3323_3325delinsCTA (MSH6)	NP_001268421.1:p.Thr1108=
NM_001281493.1:c.2807_2809delinsCTA (MSH6)	NP_001268422.1:p.Thr936=
NM_001281494.1:c.2807_2809delinsCTA (MSH6)	NP_001268423.1:p.Thr936=
XM_005264271.1:c.3416_3418delinsCTA (MSH6)	XP_005264328.1:p.Thr1139=
XM_011532798.1:c.3530_3532delinsCTA (MSH6)	XP_011531100.1:p.Thr1177=
XM_011532799.1:c.3416_3418delinsCTA (MSH6)	XP_011531101.1:p.Thr1139=
XM_011532800.1:c.3416_3418delinsCTA (MSH6)	XP_011531102.1:p.Thr1139=
XM_024452819.1:c.3713_3715delinsCTA (MSH6)	XP_024308587.1:p.Thr1238=
XM_024452820.1:c.3530_3532delinsCTA (MSH6)	XP_024308588.1:p.Thr1177=
XM_024452821.1:c.3416_3418delinsCTA (MSH6)	XP_024308589.1:p.Thr1139=
XM_024452822.1:c.2807_2809delinsCTA (MSH6)	XP_024308590.1:p.Thr936=
NM_000179.3:c.3713_3715delinsCTA (MSH6) MANE Select	NP_000170.1:p.Thr1238=
NM_001281492.2:c.3323_3325delinsCTA (MSH6)	NP_001268421.1:p.Thr1108=
NM_001281493.2:c.2807_2809delinsCTA (MSH6)	NP_001268422.1:p.Thr936=
NM_001281494.2:c.2807_2809delinsCTA (MSH6)	NP_001268423.1:p.Thr936=