Canonical Allele Identifier: CA2695200651

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 2676830
• ClinVar RCV Id: RCV003461959

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47799921_47799925delinsTATTCTT , CM000664.2:g.47799921_47799925delinsTATTCTT	GRCh38
NC_000002.11:g.48027060_48027064delinsTATTCTT , CM000664.1:g.48027060_48027064delinsTATTCTT	GRCh37
NC_000002.10:g.47880564_47880568delinsTATTCTT	NCBI36
NG_007111.1:g.21775_21779delinsTATTCTT , LRG_219:g.21775_21779delinsTATTCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.1641_1645delinsTATTCTT (MSH6)	ENSP00000406248.2:p.Lys547AsnfsTer9
ENST00000420813.6:c.1641_1645delinsTATTCTT (MSH6)	ENSP00000390382.2:p.Lys547AsnfsTer9
ENST00000455383.6:c.1641_1645delinsTATTCTT (MSH6)	ENSP00000397484.2:p.Lys547AsnfsTer9
ENST00000700004.2:c.1938_1942delinsTATTCTT (MSH6)	ENSP00000514752.2:p.Lys646AsnfsTer9
ENST00000699999.1:n.2022_2026delinsTATTCTT (MSH6)
ENST00000700000.1:c.1606+332_1606+336delinsTATTCTT (MSH6)	ENSP00000514749.1:n.1606+332_1606+336delinsTATTCTT
ENST00000700002.1:c.1944_1948delinsTATTCTT (MSH6)	ENSP00000514750.1:p.Lys648AsnfsTer9
ENST00000700003.1:c.628-3499_628-3495delinsTATTCTT (MSH6)	ENSP00000514751.1:n.628-3499_628-3495delinsTATTCTT
ENST00000700004.1:c.1095_1099delinsTATTCTT (MSH6)	ENSP00000514752.1:p.Lys365AsnfsTer9
ENST00000234420.11:c.1938_1942delinsTATTCTT (MSH6) MANE Select	ENSP00000234420.5:p.Lys646AsnfsTer9
ENST00000540021.6:c.1548_1552delinsTATTCTT (MSH6)	ENSP00000446475.1:p.Lys516AsnfsTer9
ENST00000652107.1:c.1641_1645delinsTATTCTT (MSH6)	ENSP00000498629.1:p.Lys547AsnfsTer9
ENST00000673637.1:c.1641_1645delinsTATTCTT (MSH6)	ENSP00000501310.1:p.Lys547AsnfsTer9
ENST00000234420.9:c.1938_1942delinsTATTCTT (MSH6)	ENSP00000234420.4:p.Lys646AsnfsTer9
ENST00000405808.5:c.169+8270_169+8274delinsAAGAATA (FBXO11)	ENSP00000385127.1:n.169+8270_169+8274delinsAAGAATA
ENST00000434234.5:c.*124+8069_*124+8073delinsAAGAATA (FBXO11)	ENSP00000402692.1:n.*124+8069_*124+8073delinsAAGAATA
ENST00000445503.5:c.*1285_*1289delinsTATTCTT (MSH6)	ENSP00000405294.1:n.*1285_*1289delinsTATTCTT
ENST00000538136.1:c.1032_1036delinsTATTCTT (MSH6)	ENSP00000438580.1:p.Lys344AsnfsTer9
ENST00000540021.5:c.1548_1552delinsTATTCTT (MSH6)	ENSP00000446475.1:p.Lys516AsnfsTer9
ENST00000614496.4:c.1032_1036delinsTATTCTT (MSH6)	ENSP00000477844.1:p.Lys344AsnfsTer9
ENST00000616033.4:c.1935_1939delinsTATTCTT (MSH6)	ENSP00000480261.1:p.Lys645AsnfsTer9
ENST00000622629.4:c.-1159_-1155delinsTATTCTT (MSH6)	ENSP00000482078.1:n.-1159_-1155delinsTATTCTT
NM_000179.2:c.1938_1942delinsTATTCTT , LRG_219t1:c.1938_1942delinsTATTCTT (MSH6)	NP_000170.1:p.Lys646AsnfsTer9
NM_001281492.1:c.1548_1552delinsTATTCTT (MSH6)	NP_001268421.1:p.Lys516AsnfsTer9
NM_001281493.1:c.1032_1036delinsTATTCTT (MSH6)	NP_001268422.1:p.Lys344AsnfsTer9
NM_001281494.1:c.1032_1036delinsTATTCTT (MSH6)	NP_001268423.1:p.Lys344AsnfsTer9
XM_005264271.1:c.1641_1645delinsTATTCTT (MSH6)	XP_005264328.1:p.Lys547AsnfsTer9
XM_011532798.1:c.1755_1759delinsTATTCTT (MSH6)	XP_011531100.1:p.Lys585AsnfsTer9
XM_011532799.1:c.1641_1645delinsTATTCTT (MSH6)	XP_011531101.1:p.Lys547AsnfsTer9
XM_011532800.1:c.1641_1645delinsTATTCTT (MSH6)	XP_011531102.1:p.Lys547AsnfsTer9
XM_024452819.1:c.1938_1942delinsTATTCTT (MSH6)	XP_024308587.1:p.Lys646AsnfsTer9
XM_024452820.1:c.1755_1759delinsTATTCTT (MSH6)	XP_024308588.1:p.Lys585AsnfsTer9
XM_024452821.1:c.1641_1645delinsTATTCTT (MSH6)	XP_024308589.1:p.Lys547AsnfsTer9
XM_024452822.1:c.1032_1036delinsTATTCTT (MSH6)	XP_024308590.1:p.Lys344AsnfsTer9
NM_000179.3:c.1938_1942delinsTATTCTT (MSH6) MANE Select	NP_000170.1:p.Lys646AsnfsTer9
NM_001281492.2:c.1548_1552delinsTATTCTT (MSH6)	NP_001268421.1:p.Lys516AsnfsTer9
NM_001281493.2:c.1032_1036delinsTATTCTT (MSH6)	NP_001268422.1:p.Lys344AsnfsTer9
NM_001281494.2:c.1032_1036delinsTATTCTT (MSH6)	NP_001268423.1:p.Lys344AsnfsTer9