Canonical Allele Identifier: CA769511155

Gene: MSH6 FBXO11

Linked Data

• dbSNP Id: rs1352650078
• MyVariant Identifiers: chr2:g.48027073_48027078del (hg19) ; chr2:g.47799934_47799939del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47799934_47799939del , CM000664.2:g.47799934_47799939del	GRCh38
NC_000002.11:g.48027073_48027078del , CM000664.1:g.48027073_48027078del	GRCh37
NC_000002.10:g.47880577_47880582del	NCBI36
NG_007111.1:g.21788_21793del , LRG_219:g.21788_21793del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.1654_1659del (MSH6)	ENSP00000406248.2:p.Ile552_Gly553del
ENST00000420813.6:c.1654_1659del (MSH6)	ENSP00000390382.2:p.Ile552_Gly553del
ENST00000455383.6:c.1654_1659del (MSH6)	ENSP00000397484.2:p.Ile552_Gly553del
ENST00000700004.2:c.1951_1956del (MSH6)	ENSP00000514752.2:p.Ile651_Gly652del
ENST00000699999.1:n.2035_2040del (MSH6)
ENST00000700000.1:c.1606+345_1606+350del (MSH6)	ENSP00000514749.1:n.1606+345_1606+350del
ENST00000700002.1:c.1957_1962del (MSH6)	ENSP00000514750.1:p.Ile653_Gly654del
ENST00000700003.1:c.628-3486_628-3481del (MSH6)	ENSP00000514751.1:n.628-3486_628-3481del
ENST00000700004.1:c.1108_1113del (MSH6)	ENSP00000514752.1:p.Ile370_Gly371del
ENST00000234420.11:c.1951_1956del (MSH6) MANE Select	ENSP00000234420.5:p.Ile651_Gly652del
ENST00000540021.6:c.1561_1566del (MSH6)	ENSP00000446475.1:p.Ile521_Gly522del
ENST00000652107.1:c.1654_1659del (MSH6)	ENSP00000498629.1:p.Ile552_Gly553del
ENST00000673637.1:c.1654_1659del (MSH6)	ENSP00000501310.1:p.Ile552_Gly553del
ENST00000234420.9:c.1951_1956del (MSH6)	ENSP00000234420.4:p.Ile651_Gly652del
ENST00000405808.5:c.169+8256_169+8261del (FBXO11)	ENSP00000385127.1:n.169+8256_169+8261del
ENST00000434234.5:c.*124+8055_*124+8060del (FBXO11)	ENSP00000402692.1:n.*124+8055_*124+8060del
ENST00000445503.5:c.*1298_*1303del (MSH6)	ENSP00000405294.1:n.*1298_*1303del
ENST00000538136.1:c.1045_1050del (MSH6)	ENSP00000438580.1:p.Ile349_Gly350del
ENST00000540021.5:c.1561_1566del (MSH6)	ENSP00000446475.1:p.Ile521_Gly522del
ENST00000614496.4:c.1045_1050del (MSH6)	ENSP00000477844.1:p.Ile349_Gly350del
ENST00000616033.4:c.1948_1953del (MSH6)	ENSP00000480261.1:p.Ile650_Gly651del
ENST00000622629.4:c.-1146_-1141del (MSH6)	ENSP00000482078.1:n.-1146_-1141del
NM_000179.2:c.1951_1956del , LRG_219t1:c.1951_1956del (MSH6)	NP_000170.1:p.Ile651_Gly652del
NM_001281492.1:c.1561_1566del (MSH6)	NP_001268421.1:p.Ile521_Gly522del
NM_001281493.1:c.1045_1050del (MSH6)	NP_001268422.1:p.Ile349_Gly350del
NM_001281494.1:c.1045_1050del (MSH6)	NP_001268423.1:p.Ile349_Gly350del
XM_005264271.1:c.1654_1659del (MSH6)	XP_005264328.1:p.Ile552_Gly553del
XM_011532798.1:c.1768_1773del (MSH6)	XP_011531100.1:p.Ile590_Gly591del
XM_011532799.1:c.1654_1659del (MSH6)	XP_011531101.1:p.Ile552_Gly553del
XM_011532800.1:c.1654_1659del (MSH6)	XP_011531102.1:p.Ile552_Gly553del
XM_024452819.1:c.1951_1956del (MSH6)	XP_024308587.1:p.Ile651_Gly652del
XM_024452820.1:c.1768_1773del (MSH6)	XP_024308588.1:p.Ile590_Gly591del
XM_024452821.1:c.1654_1659del (MSH6)	XP_024308589.1:p.Ile552_Gly553del
XM_024452822.1:c.1045_1050del (MSH6)	XP_024308590.1:p.Ile349_Gly350del
NM_000179.3:c.1951_1956del (MSH6) MANE Select	NP_000170.1:p.Ile651_Gly652del
NM_001281492.2:c.1561_1566del (MSH6)	NP_001268421.1:p.Ile521_Gly522del
NM_001281493.2:c.1045_1050del (MSH6)	NP_001268422.1:p.Ile349_Gly350del
NM_001281494.2:c.1045_1050del (MSH6)	NP_001268423.1:p.Ile349_Gly350del