Canonical Allele Identifier: CA2496053476

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47805634_47805635delinsTG , CM000664.2:g.47805634_47805635delinsTG	GRCh38
NC_000002.11:g.48032773_48032774delinsTG , CM000664.1:g.48032773_48032774delinsTG	GRCh37
NC_000002.10:g.47886277_47886278delinsTG	NCBI36
NG_007111.1:g.27488_27489delinsTG , LRG_219:g.27488_27489delinsTG
NG_008397.1:g.105041_105042delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3276_3277delinsTG (MSH6)	ENSP00000406248.2:p.Phe1092=
ENST00000420813.6:c.3276_3277delinsTG (MSH6)	ENSP00000390382.2:p.Phe1092=
ENST00000455383.6:c.3276_3277delinsTG (MSH6)	ENSP00000397484.2:p.Phe1092=
ENST00000700004.2:c.3189_3190delinsTG (MSH6)	ENSP00000514752.2:p.Phe1063=
ENST00000699999.1:n.4247_4248delinsTG (MSH6)
ENST00000700000.1:c.2007_2008delinsTG (MSH6)	ENSP00000514749.1:p.Phe669=
ENST00000700002.1:c.3579_3580delinsTG (MSH6)	ENSP00000514750.1:p.Phe1193=
ENST00000700003.1:c.1028_1029delinsTG (MSH6)	ENSP00000514751.1:n.1028_1029delinsTG
ENST00000700004.1:c.2346_2347delinsTG (MSH6)	ENSP00000514752.1:p.Phe782=
ENST00000700005.1:n.2424_2425delinsTG (MSH6)
ENST00000700006.1:n.4235_4236delinsTG (MSH6)
ENST00000700007.1:n.2168_2169delinsTG (MSH6)
ENST00000700008.1:n.1742_1743delinsTG (MSH6)
ENST00000700009.1:n.1741_1742delinsTG (MSH6)
ENST00000700010.1:n.982_983delinsTG (MSH6)
ENST00000700011.1:n.2867_2868delinsTG (MSH6)
ENST00000234420.11:c.3573_3574delinsTG (MSH6) MANE Select	ENSP00000234420.5:p.Phe1191=
ENST00000540021.6:c.3183_3184delinsTG (MSH6)	ENSP00000446475.1:p.Phe1061=
ENST00000652107.1:c.3276_3277delinsTG (MSH6)	ENSP00000498629.1:p.Phe1092=
ENST00000673637.1:c.3276_3277delinsTG (MSH6)	ENSP00000501310.1:p.Phe1092=
ENST00000234420.9:c.3573_3574delinsTG (MSH6)	ENSP00000234420.4:p.Phe1191=
ENST00000405808.5:c.169+2560_169+2561delinsCA (FBXO11)	ENSP00000385127.1:n.169+2560_169+2561delinsCA
ENST00000434234.5:c.*124+2359_*124+2360delinsCA (FBXO11)	ENSP00000402692.1:n.*124+2359_*124+2360delinsCA
ENST00000445503.5:c.*2920_*2921delinsTG (MSH6)	ENSP00000405294.1:n.*2920_*2921delinsTG
ENST00000538136.1:c.2667_2668delinsTG (MSH6)	ENSP00000438580.1:p.Phe889=
ENST00000540021.5:c.3183_3184delinsTG (MSH6)	ENSP00000446475.1:p.Phe1061=
ENST00000614496.4:c.2667_2668delinsTG (MSH6)	ENSP00000477844.1:p.Phe889=
ENST00000622629.4:c.477_478delinsTG (MSH6)	ENSP00000482078.1:p.Phe159=
NM_000179.2:c.3573_3574delinsTG , LRG_219t1:c.3573_3574delinsTG (MSH6)	NP_000170.1:p.Phe1191=
NM_001281492.1:c.3183_3184delinsTG (MSH6)	NP_001268421.1:p.Phe1061=
NM_001281493.1:c.2667_2668delinsTG (MSH6)	NP_001268422.1:p.Phe889=
NM_001281494.1:c.2667_2668delinsTG (MSH6)	NP_001268423.1:p.Phe889=
XM_005264271.1:c.3276_3277delinsTG (MSH6)	XP_005264328.1:p.Phe1092=
XM_011532798.1:c.3390_3391delinsTG (MSH6)	XP_011531100.1:p.Phe1130=
XM_011532799.1:c.3276_3277delinsTG (MSH6)	XP_011531101.1:p.Phe1092=
XM_011532800.1:c.3276_3277delinsTG (MSH6)	XP_011531102.1:p.Phe1092=
XM_024452819.1:c.3573_3574delinsTG (MSH6)	XP_024308587.1:p.Phe1191=
XM_024452820.1:c.3390_3391delinsTG (MSH6)	XP_024308588.1:p.Phe1130=
XM_024452821.1:c.3276_3277delinsTG (MSH6)	XP_024308589.1:p.Phe1092=
XM_024452822.1:c.2667_2668delinsTG (MSH6)	XP_024308590.1:p.Phe889=
NM_000179.3:c.3573_3574delinsTG (MSH6) MANE Select	NP_000170.1:p.Phe1191=
NM_001281492.2:c.3183_3184delinsTG (MSH6)	NP_001268421.1:p.Phe1061=
NM_001281493.2:c.2667_2668delinsTG (MSH6)	NP_001268422.1:p.Phe889=
NM_001281494.2:c.2667_2668delinsTG (MSH6)	NP_001268423.1:p.Phe889=