Canonical Allele Identifier: CA2658967968

Gene: MSH6 FBXO11

Linked Data

• gnomAD v4: 2-47806397-TGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806401_47806402del , CM000664.2:g.47806401_47806402del	GRCh38
NC_000002.11:g.48033540_48033541del , CM000664.1:g.48033540_48033541del	GRCh37
NC_000002.10:g.47887044_47887045del	NCBI36
NG_007111.1:g.28255_28256del , LRG_219:g.28255_28256del
NG_008397.1:g.104277_104278del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3504+43_3504+44del (MSH6)	ENSP00000406248.2:n.3504+43_3504+44del
ENST00000420813.6:c.3504+43_3504+44del (MSH6)	ENSP00000390382.2:n.3504+43_3504+44del
ENST00000455383.6:c.3504+43_3504+44del (MSH6)	ENSP00000397484.2:n.3504+43_3504+44del
ENST00000700004.2:c.3417+43_3417+44del (MSH6)	ENSP00000514752.2:n.3417+43_3417+44del
ENST00000699999.1:n.4475+43_4475+44del (MSH6)
ENST00000700000.1:c.2235+43_2235+44del (MSH6)	ENSP00000514749.1:n.2235+43_2235+44del
ENST00000700002.1:c.3807+43_3807+44del (MSH6)	ENSP00000514750.1:n.3807+43_3807+44del
ENST00000700003.1:c.1256+43_1256+44del (MSH6)	ENSP00000514751.1:n.1256+43_1256+44del
ENST00000700004.1:c.2574+43_2574+44del (MSH6)	ENSP00000514752.1:n.2574+43_2574+44del
ENST00000700005.1:n.2652+43_2652+44del (MSH6)
ENST00000700006.1:n.4959+43_4959+44del (MSH6)
ENST00000700007.1:n.2396+43_2396+44del (MSH6)
ENST00000700008.1:n.2013_2014del (MSH6)
ENST00000700009.1:n.2465+43_2465+44del (MSH6)
ENST00000700010.1:n.1210+43_1210+44del (MSH6)
ENST00000700011.1:n.3095+43_3095+44del (MSH6)
ENST00000682451.1:n.4349_4350del (FBXO11)
ENST00000684712.1:n.4611_4612del (FBXO11)
ENST00000234420.11:c.3801+43_3801+44del (MSH6) MANE Select	ENSP00000234420.5:n.3801+43_3801+44del
ENST00000540021.6:c.3411+43_3411+44del (MSH6)	ENSP00000446475.1:n.3411+43_3411+44del
ENST00000652107.1:c.3504+43_3504+44del (MSH6)	ENSP00000498629.1:n.3504+43_3504+44del
ENST00000673637.1:c.3504+43_3504+44del (MSH6)	ENSP00000501310.1:n.3504+43_3504+44del
ENST00000234420.9:c.3801+43_3801+44del (MSH6)	ENSP00000234420.4:n.3801+43_3801+44del
ENST00000405808.5:c.169+1796_169+1797del (FBXO11)	ENSP00000385127.1:n.169+1796_169+1797del
ENST00000434234.5:c.*124+1595_*124+1596del (FBXO11)	ENSP00000402692.1:n.*124+1595_*124+1596del
ENST00000445503.5:c.*3148+43_*3148+44del (MSH6)	ENSP00000405294.1:n.*3148+43_*3148+44del
ENST00000538136.1:c.2895+43_2895+44del (MSH6)	ENSP00000438580.1:n.2895+43_2895+44del
ENST00000540021.5:c.3411+43_3411+44del (MSH6)	ENSP00000446475.1:n.3411+43_3411+44del
ENST00000614496.4:c.2895+43_2895+44del (MSH6)	ENSP00000477844.1:n.2895+43_2895+44del
ENST00000622629.4:c.702+43_702+44del (MSH6)	ENSP00000482078.1:n.702+43_702+44del
NM_000179.2:c.3801+43_3801+44del , LRG_219t1:c.3801+43_3801+44del (MSH6)	NP_000170.1:n.3801+43_3801+44del
NM_001281492.1:c.3411+43_3411+44del (MSH6)	NP_001268421.1:n.3411+43_3411+44del
NM_001281493.1:c.2895+43_2895+44del (MSH6)	NP_001268422.1:n.2895+43_2895+44del
NM_001281494.1:c.2895+43_2895+44del (MSH6)	NP_001268423.1:n.2895+43_2895+44del
XM_005264271.1:c.3504+43_3504+44del (MSH6)	XP_005264328.1:n.3504+43_3504+44del
XM_011532798.1:c.3618+43_3618+44del (MSH6)	XP_011531100.1:n.3618+43_3618+44del
XM_011532799.1:c.3504+43_3504+44del (MSH6)	XP_011531101.1:n.3504+43_3504+44del
XM_011532800.1:c.3504+43_3504+44del (MSH6)	XP_011531102.1:n.3504+43_3504+44del
XM_024452819.1:c.3844_3845del (MSH6)	XP_024308587.1:p.Arg1282GlyfsTer16
XM_024452820.1:c.3661_3662del (MSH6)	XP_024308588.1:p.Arg1221GlyfsTer16
XM_024452821.1:c.3547_3548del (MSH6)	XP_024308589.1:p.Arg1183GlyfsTer16
XM_024452822.1:c.2938_2939del (MSH6)	XP_024308590.1:p.Arg980GlyfsTer16
NM_000179.3:c.3801+43_3801+44del (MSH6) MANE Select	NP_000170.1:n.3801+43_3801+44del
NM_001281492.2:c.3411+43_3411+44del (MSH6)	NP_001268421.1:n.3411+43_3411+44del
NM_001281493.2:c.2895+43_2895+44del (MSH6)	NP_001268422.1:n.2895+43_2895+44del
NM_001281494.2:c.2895+43_2895+44del (MSH6)	NP_001268423.1:n.2895+43_2895+44del