Canonical Allele Identifier: CA46710486

Gene: MSH6 FBXO11

Linked Data

• dbSNP Id: rs63749941
• MyVariant Identifiers: chr2:g.48027287_48027307del (hg19) ; chr2:g.47800148_47800168del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47800149_47800169del , CM000664.2:g.47800149_47800169del	GRCh38
NC_000002.11:g.48027288_48027308del , CM000664.1:g.48027288_48027308del	GRCh37
NC_000002.10:g.47880792_47880812del	NCBI36
NG_007111.1:g.22003_22023del , LRG_219:g.22003_22023del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.1869_1889del (MSH6)	ENSP00000406248.2:p.Gly624_Ala630del
ENST00000420813.6:c.1869_1889del (MSH6)	ENSP00000390382.2:p.Gly624_Ala630del
ENST00000455383.6:c.1869_1889del (MSH6)	ENSP00000397484.2:p.Gly624_Ala630del
ENST00000700004.2:c.2166_2186del (MSH6)	ENSP00000514752.2:p.Gly723_Ala729del
ENST00000699999.1:n.2250_2270del (MSH6)
ENST00000700000.1:c.1606+560_1606+580del (MSH6)	ENSP00000514749.1:n.1606+560_1606+580del
ENST00000700002.1:c.2172_2192del (MSH6)	ENSP00000514750.1:p.Gly725_Ala731del
ENST00000700003.1:c.628-3271_628-3251del (MSH6)	ENSP00000514751.1:n.628-3271_628-3251del
ENST00000700004.1:c.1323_1343del (MSH6)	ENSP00000514752.1:p.Gly442_Ala448del
ENST00000234420.11:c.2166_2186del (MSH6) MANE Select	ENSP00000234420.5:p.Gly723_Ala729del
ENST00000540021.6:c.1776_1796del (MSH6)	ENSP00000446475.1:p.Gly593_Ala599del
ENST00000652107.1:c.1869_1889del (MSH6)	ENSP00000498629.1:p.Gly624_Ala630del
ENST00000673637.1:c.1869_1889del (MSH6)	ENSP00000501310.1:p.Gly624_Ala630del
ENST00000234420.9:c.2166_2186del (MSH6)	ENSP00000234420.4:p.Gly723_Ala729del
ENST00000405808.5:c.169+8027_169+8047del (FBXO11)	ENSP00000385127.1:n.169+8027_169+8047del
ENST00000434234.5:c.*124+7826_*124+7846del (FBXO11)	ENSP00000402692.1:n.*124+7826_*124+7846del
ENST00000445503.5:c.*1513_*1533del (MSH6)	ENSP00000405294.1:n.*1513_*1533del
ENST00000538136.1:c.1260_1280del (MSH6)	ENSP00000438580.1:p.Gly421_Ala427del
ENST00000540021.5:c.1776_1796del (MSH6)	ENSP00000446475.1:p.Gly593_Ala599del
ENST00000614496.4:c.1260_1280del (MSH6)	ENSP00000477844.1:p.Gly421_Ala427del
ENST00000616033.4:c.2163_2183del (MSH6)	ENSP00000480261.1:p.Gly722_Ala728del
ENST00000622629.4:c.-931_-911del (MSH6)	ENSP00000482078.1:n.-931_-911del
NM_000179.2:c.2166_2186del , LRG_219t1:c.2166_2186del (MSH6)	NP_000170.1:p.Gly723_Ala729del
NM_001281492.1:c.1776_1796del (MSH6)	NP_001268421.1:p.Gly593_Ala599del
NM_001281493.1:c.1260_1280del (MSH6)	NP_001268422.1:p.Gly421_Ala427del
NM_001281494.1:c.1260_1280del (MSH6)	NP_001268423.1:p.Gly421_Ala427del
XM_005264271.1:c.1869_1889del (MSH6)	XP_005264328.1:p.Gly624_Ala630del
XM_011532798.1:c.1983_2003del (MSH6)	XP_011531100.1:p.Gly662_Ala668del
XM_011532799.1:c.1869_1889del (MSH6)	XP_011531101.1:p.Gly624_Ala630del
XM_011532800.1:c.1869_1889del (MSH6)	XP_011531102.1:p.Gly624_Ala630del
XM_024452819.1:c.2166_2186del (MSH6)	XP_024308587.1:p.Gly723_Ala729del
XM_024452820.1:c.1983_2003del (MSH6)	XP_024308588.1:p.Gly662_Ala668del
XM_024452821.1:c.1869_1889del (MSH6)	XP_024308589.1:p.Gly624_Ala630del
XM_024452822.1:c.1260_1280del (MSH6)	XP_024308590.1:p.Gly421_Ala427del
NM_000179.3:c.2166_2186del (MSH6) MANE Select	NP_000170.1:p.Gly723_Ala729del
NM_001281492.2:c.1776_1796del (MSH6)	NP_001268421.1:p.Gly593_Ala599del
NM_001281493.2:c.1260_1280del (MSH6)	NP_001268422.1:p.Gly421_Ala427del
NM_001281494.2:c.1260_1280del (MSH6)	NP_001268423.1:p.Gly421_Ala427del