Canonical Allele Identifier: CA2496054242

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806357_47806358delinsTG , CM000664.2:g.47806357_47806358delinsTG	GRCh38
NC_000002.11:g.48033496_48033497delinsTG , CM000664.1:g.48033496_48033497delinsTG	GRCh37
NC_000002.10:g.47887000_47887001delinsTG	NCBI36
NG_007111.1:g.28211_28212delinsTG , LRG_219:g.28211_28212delinsTG
NG_008397.1:g.104318_104319delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.3503_3504delinsTG (MSH6)	ENSP00000406248.2:p.Met1168=
ENST00000420813.6:c.3503_3504delinsTG (MSH6)	ENSP00000390382.2:p.Met1168=
ENST00000455383.6:c.3503_3504delinsTG (MSH6)	ENSP00000397484.2:p.Met1168=
ENST00000700004.2:c.3416_3417delinsTG (MSH6)	ENSP00000514752.2:p.Met1139=
ENST00000699999.1:n.4474_4475delinsTG (MSH6)
ENST00000700000.1:c.2234_2235delinsTG (MSH6)	ENSP00000514749.1:p.Met745=
ENST00000700002.1:c.3806_3807delinsTG (MSH6)	ENSP00000514750.1:p.Met1269=
ENST00000700003.1:c.1255_1256delinsTG (MSH6)	ENSP00000514751.1:n.1255_1256delinsTG
ENST00000700004.1:c.2573_2574delinsTG (MSH6)	ENSP00000514752.1:p.Met858=
ENST00000700005.1:n.2651_2652delinsTG (MSH6)
ENST00000700006.1:n.4958_4959delinsTG (MSH6)
ENST00000700007.1:n.2395_2396delinsTG (MSH6)
ENST00000700008.1:n.1969_1970delinsTG (MSH6)
ENST00000700009.1:n.2464_2465delinsTG (MSH6)
ENST00000700010.1:n.1209_1210delinsTG (MSH6)
ENST00000700011.1:n.3094_3095delinsTG (MSH6)
ENST00000682451.1:n.4390_4391delinsCA (FBXO11)
ENST00000684712.1:n.4652_4653delinsCA (FBXO11)
ENST00000234420.11:c.3800_3801delinsTG (MSH6) MANE Select	ENSP00000234420.5:p.Met1267=
ENST00000540021.6:c.3410_3411delinsTG (MSH6)	ENSP00000446475.1:p.Met1137=
ENST00000652107.1:c.3503_3504delinsTG (MSH6)	ENSP00000498629.1:p.Met1168=
ENST00000673637.1:c.3503_3504delinsTG (MSH6)	ENSP00000501310.1:p.Met1168=
ENST00000234420.9:c.3800_3801delinsTG (MSH6)	ENSP00000234420.4:p.Met1267=
ENST00000405808.5:c.169+1837_169+1838delinsCA (FBXO11)	ENSP00000385127.1:n.169+1837_169+1838deli...
ENST00000434234.5:c.*124+1636_*124+1637delinsCA (FBXO11)	ENSP00000402692.1:n.*124+1636_*124+1637de...
ENST00000445503.5:c.*3147_*3148delinsTG (MSH6)	ENSP00000405294.1:n.*3147_*3148delinsTG
ENST00000538136.1:c.2894_2895delinsTG (MSH6)	ENSP00000438580.1:p.Met965=
ENST00000540021.5:c.3410_3411delinsTG (MSH6)	ENSP00000446475.1:p.Met1137=
ENST00000614496.4:c.2894_2895delinsTG (MSH6)	ENSP00000477844.1:p.Met965=
ENST00000622629.4:c.701_702delinsTG (MSH6)	ENSP00000482078.1:p.Met234=
NM_000179.2:c.3800_3801delinsTG , LRG_219t1:c.3800_3801delinsTG (MSH6)	NP_000170.1:p.Met1267=
NM_001281492.1:c.3410_3411delinsTG (MSH6)	NP_001268421.1:p.Met1137=
NM_001281493.1:c.2894_2895delinsTG (MSH6)	NP_001268422.1:p.Met965=
NM_001281494.1:c.2894_2895delinsTG (MSH6)	NP_001268423.1:p.Met965=
XM_005264271.1:c.3503_3504delinsTG (MSH6)	XP_005264328.1:p.Met1168=
XM_011532798.1:c.3617_3618delinsTG (MSH6)	XP_011531100.1:p.Met1206=
XM_011532799.1:c.3503_3504delinsTG (MSH6)	XP_011531101.1:p.Met1168=
XM_011532800.1:c.3503_3504delinsTG (MSH6)	XP_011531102.1:p.Met1168=
XM_024452819.1:c.3800_3801delinsTG (MSH6)	XP_024308587.1:p.Met1267=
XM_024452820.1:c.3617_3618delinsTG (MSH6)	XP_024308588.1:p.Met1206=
XM_024452821.1:c.3503_3504delinsTG (MSH6)	XP_024308589.1:p.Met1168=
XM_024452822.1:c.2894_2895delinsTG (MSH6)	XP_024308590.1:p.Met965=
NM_000179.3:c.3800_3801delinsTG (MSH6) MANE Select	NP_000170.1:p.Met1267=
NM_001281492.2:c.3410_3411delinsTG (MSH6)	NP_001268421.1:p.Met1137=
NM_001281493.2:c.2894_2895delinsTG (MSH6)	NP_001268422.1:p.Met965=
NM_001281494.2:c.2894_2895delinsTG (MSH6)	NP_001268423.1:p.Met965=