Canonical Allele Identifier: CA913187451

Gene: MSH6 FBXO11

Linked Data

• dbSNP Id: rs1669512610

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47800786_47800797del , CM000664.2:g.47800786_47800797del	GRCh38
NC_000002.11:g.48027925_48027936del , CM000664.1:g.48027925_48027936del	GRCh37
NC_000002.10:g.47881429_47881440del	NCBI36
NG_007111.1:g.22640_22651del , LRG_219:g.22640_22651del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.2506_2517del (MSH6)	ENSP00000406248.2:p.Ser836_Asp839del
ENST00000420813.6:c.2506_2517del (MSH6)	ENSP00000390382.2:p.Ser836_Asp839del
ENST00000455383.6:c.2506_2517del (MSH6)	ENSP00000397484.2:p.Ser836_Asp839del
ENST00000700004.2:c.2803_2814del (MSH6)	ENSP00000514752.2:p.Ser935_Asp938del
ENST00000699999.1:n.2887_2898del (MSH6)
ENST00000700000.1:c.1606+1197_1606+1208del (MSH6)	ENSP00000514749.1:n.1606+1197_1606+1208del
ENST00000700002.1:c.2809_2820del (MSH6)	ENSP00000514750.1:p.Ser937_Asp940del
ENST00000700003.1:c.628-2634_628-2623del (MSH6)	ENSP00000514751.1:n.628-2634_628-2623del
ENST00000700004.1:c.1960_1971del (MSH6)	ENSP00000514752.1:p.Ser654_Asp657del
ENST00000234420.11:c.2803_2814del (MSH6) MANE Select	ENSP00000234420.5:p.Ser935_Asp938del
ENST00000540021.6:c.2413_2424del (MSH6)	ENSP00000446475.1:p.Ser805_Asp808del
ENST00000652107.1:c.2506_2517del (MSH6)	ENSP00000498629.1:p.Ser836_Asp839del
ENST00000673637.1:c.2506_2517del (MSH6)	ENSP00000501310.1:p.Ser836_Asp839del
ENST00000234420.9:c.2803_2814del (MSH6)	ENSP00000234420.4:p.Ser935_Asp938del
ENST00000405808.5:c.169+7402_169+7413del (FBXO11)	ENSP00000385127.1:n.169+7402_169+7413del
ENST00000434234.5:c.*124+7201_*124+7212del (FBXO11)	ENSP00000402692.1:n.*124+7201_*124+7212del
ENST00000445503.5:c.*2150_*2161del (MSH6)	ENSP00000405294.1:n.*2150_*2161del
ENST00000538136.1:c.1897_1908del (MSH6)	ENSP00000438580.1:p.Ser633_Asp636del
ENST00000540021.5:c.2413_2424del (MSH6)	ENSP00000446475.1:p.Ser805_Asp808del
ENST00000614496.4:c.1897_1908del (MSH6)	ENSP00000477844.1:p.Ser633_Asp636del
ENST00000616033.4:c.2800_2811del (MSH6)	ENSP00000480261.1:p.Ser934_Asp937del
ENST00000622629.4:c.-294_-283del (MSH6)	ENSP00000482078.1:n.-294_-283del
NM_000179.2:c.2803_2814del , LRG_219t1:c.2803_2814del (MSH6)	NP_000170.1:p.Ser935_Asp938del
NM_001281492.1:c.2413_2424del (MSH6)	NP_001268421.1:p.Ser805_Asp808del
NM_001281493.1:c.1897_1908del (MSH6)	NP_001268422.1:p.Ser633_Asp636del
NM_001281494.1:c.1897_1908del (MSH6)	NP_001268423.1:p.Ser633_Asp636del
XM_005264271.1:c.2506_2517del (MSH6)	XP_005264328.1:p.Ser836_Asp839del
XM_011532798.1:c.2620_2631del (MSH6)	XP_011531100.1:p.Ser874_Asp877del
XM_011532799.1:c.2506_2517del (MSH6)	XP_011531101.1:p.Ser836_Asp839del
XM_011532800.1:c.2506_2517del (MSH6)	XP_011531102.1:p.Ser836_Asp839del
XM_024452819.1:c.2803_2814del (MSH6)	XP_024308587.1:p.Ser935_Asp938del
XM_024452820.1:c.2620_2631del (MSH6)	XP_024308588.1:p.Ser874_Asp877del
XM_024452821.1:c.2506_2517del (MSH6)	XP_024308589.1:p.Ser836_Asp839del
XM_024452822.1:c.1897_1908del (MSH6)	XP_024308590.1:p.Ser633_Asp636del
NM_000179.3:c.2803_2814del (MSH6) MANE Select	NP_000170.1:p.Ser935_Asp938del
NM_001281492.2:c.2413_2424del (MSH6)	NP_001268421.1:p.Ser805_Asp808del
NM_001281493.2:c.1897_1908del (MSH6)	NP_001268422.1:p.Ser633_Asp636del
NM_001281494.2:c.1897_1908del (MSH6)	NP_001268423.1:p.Ser633_Asp636del