Canonical Allele Identifier: CA891841783

Gene: MSH6 FBXO11

Linked Data

• dbSNP Id: rs2104386655

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47800042_47800043insCTACCTCAAAA , CM000664.2:g.47800042_47800043insCTACCTCAAAA	GRCh38
NC_000002.11:g.48027181_48027182insCTACCTCAAAA , CM000664.1:g.48027181_48027182insCTACCTCAAAA	GRCh37
NC_000002.10:g.47880685_47880686insCTACCTCAAAA	NCBI36
NG_007111.1:g.21896_21897insCTACCTCAAAA , LRG_219:g.21896_21897insCTACCTCAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.1762_1763insCTACCTCAAAA (MSH6)	ENSP00000406248.2:p.Cys588SerfsTer?
ENST00000420813.6:c.1762_1763insCTACCTCAAAA (MSH6)	ENSP00000390382.2:p.Cys588SerfsTer?
ENST00000455383.6:c.1762_1763insCTACCTCAAAA (MSH6)	ENSP00000397484.2:p.Cys588SerfsTer?
ENST00000700004.2:c.2059_2060insCTACCTCAAAA (MSH6)	ENSP00000514752.2:p.Cys687SerfsTer?
ENST00000699999.1:n.2143_2144insCTACCTCAAAA (MSH6)
ENST00000700000.1:c.1606+453_1606+454insCTACCTCAAAA (MSH6)	ENSP00000514749.1:n.1606+453_1606+454insCTACCTCAAAA
ENST00000700002.1:c.2065_2066insCTACCTCAAAA (MSH6)	ENSP00000514750.1:p.Cys689SerfsTer?
ENST00000700003.1:c.628-3378_628-3377insCTACCTCAAAA (MSH6)	ENSP00000514751.1:n.628-3378_628-3377insCTACCTCAAAA
ENST00000700004.1:c.1216_1217insCTACCTCAAAA (MSH6)	ENSP00000514752.1:p.Cys406SerfsTer?
ENST00000234420.11:c.2059_2060insCTACCTCAAAA (MSH6) MANE Select	ENSP00000234420.5:p.Cys687SerfsTer?
ENST00000540021.6:c.1669_1670insCTACCTCAAAA (MSH6)	ENSP00000446475.1:p.Cys557SerfsTer?
ENST00000652107.1:c.1762_1763insCTACCTCAAAA (MSH6)	ENSP00000498629.1:p.Cys588SerfsTer?
ENST00000673637.1:c.1762_1763insCTACCTCAAAA (MSH6)	ENSP00000501310.1:p.Cys588SerfsTer?
ENST00000234420.9:c.2059_2060insCTACCTCAAAA (MSH6)	ENSP00000234420.4:p.Cys687SerfsTer?
ENST00000405808.5:c.169+8152_169+8153insTTTTGAGGTAG (FBXO11)	ENSP00000385127.1:n.169+8152_169+8153insTTTTGAGGTAG
ENST00000434234.5:c.*124+7951_*124+7952insTTTTGAGGTAG (FBXO11)	ENSP00000402692.1:n.*124+7951_*124+7952insTTTTGAGGTAG
ENST00000445503.5:c.*1406_*1407insCTACCTCAAAA (MSH6)	ENSP00000405294.1:n.*1406_*1407insCTACCTCAAAA
ENST00000538136.1:c.1153_1154insCTACCTCAAAA (MSH6)	ENSP00000438580.1:p.Cys385SerfsTer?
ENST00000540021.5:c.1669_1670insCTACCTCAAAA (MSH6)	ENSP00000446475.1:p.Cys557SerfsTer?
ENST00000614496.4:c.1153_1154insCTACCTCAAAA (MSH6)	ENSP00000477844.1:p.Cys385SerfsTer?
ENST00000616033.4:c.2056_2057insCTACCTCAAAA (MSH6)	ENSP00000480261.1:p.Cys686SerfsTer?
ENST00000622629.4:c.-1038_-1037insCTACCTCAAAA (MSH6)	ENSP00000482078.1:n.-1038_-1037insCTACCTCAAAA
NM_000179.2:c.2059_2060insCTACCTCAAAA , LRG_219t1:c.2059_2060insCTACCTCAAAA (MSH6)	NP_000170.1:p.Cys687SerfsTer?
NM_001281492.1:c.1669_1670insCTACCTCAAAA (MSH6)	NP_001268421.1:p.Cys557SerfsTer?
NM_001281493.1:c.1153_1154insCTACCTCAAAA (MSH6)	NP_001268422.1:p.Cys385SerfsTer?
NM_001281494.1:c.1153_1154insCTACCTCAAAA (MSH6)	NP_001268423.1:p.Cys385SerfsTer?
XM_005264271.1:c.1762_1763insCTACCTCAAAA (MSH6)	XP_005264328.1:p.Cys588SerfsTer?
XM_011532798.1:c.1876_1877insCTACCTCAAAA (MSH6)	XP_011531100.1:p.Cys626SerfsTer?
XM_011532799.1:c.1762_1763insCTACCTCAAAA (MSH6)	XP_011531101.1:p.Cys588SerfsTer?
XM_011532800.1:c.1762_1763insCTACCTCAAAA (MSH6)	XP_011531102.1:p.Cys588SerfsTer?
XM_024452819.1:c.2059_2060insCTACCTCAAAA (MSH6)	XP_024308587.1:p.Cys687SerfsTer?
XM_024452820.1:c.1876_1877insCTACCTCAAAA (MSH6)	XP_024308588.1:p.Cys626SerfsTer?
XM_024452821.1:c.1762_1763insCTACCTCAAAA (MSH6)	XP_024308589.1:p.Cys588SerfsTer?
XM_024452822.1:c.1153_1154insCTACCTCAAAA (MSH6)	XP_024308590.1:p.Cys385SerfsTer?
NM_000179.3:c.2059_2060insCTACCTCAAAA (MSH6) MANE Select	NP_000170.1:p.Cys687SerfsTer?
NM_001281492.2:c.1669_1670insCTACCTCAAAA (MSH6)	NP_001268421.1:p.Cys557SerfsTer?
NM_001281493.2:c.1153_1154insCTACCTCAAAA (MSH6)	NP_001268422.1:p.Cys385SerfsTer?
NM_001281494.2:c.1153_1154insCTACCTCAAAA (MSH6)	NP_001268423.1:p.Cys385SerfsTer?