Canonical Allele Identifier: CA2496048854

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47799613_47799617delinsGAAAA , CM000664.2:g.47799613_47799617delinsGAAAA	GRCh38
NC_000002.11:g.48026752_48026756delinsGAAAA , CM000664.1:g.48026752_48026756delinsGAAAA	GRCh37
NC_000002.10:g.47880256_47880260delinsGAAAA	NCBI36
NG_007111.1:g.21467_21471delinsGAAAA , LRG_219:g.21467_21471delinsGAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.1333_1337delinsGAAAA (MSH6)	ENSP00000406248.2:p.Glu445=
ENST00000420813.6:c.1333_1337delinsGAAAA (MSH6)	ENSP00000390382.2:p.Glu445=
ENST00000455383.6:c.1333_1337delinsGAAAA (MSH6)	ENSP00000397484.2:p.Glu445=
ENST00000700004.2:c.1630_1634delinsGAAAA (MSH6)	ENSP00000514752.2:p.Glu544=
ENST00000699999.1:n.1714_1718delinsGAAAA (MSH6)
ENST00000700000.1:c.1606+24_1606+28delinsGAAAA (MSH6)	ENSP00000514749.1:n.1606+24_1606+28delinsGAAAA
ENST00000700002.1:c.1636_1640delinsGAAAA (MSH6)	ENSP00000514750.1:p.Glu546=
ENST00000700003.1:c.627+3550_627+3554delinsGAAAA (MSH6)	ENSP00000514751.1:n.627+3550_627+3554delinsGAAAA
ENST00000700004.1:c.787_791delinsGAAAA (MSH6)	ENSP00000514752.1:p.Glu263=
ENST00000234420.11:c.1630_1634delinsGAAAA (MSH6) MANE Select	ENSP00000234420.5:p.Glu544=
ENST00000540021.6:c.1240_1244delinsGAAAA (MSH6)	ENSP00000446475.1:p.Glu414=
ENST00000652107.1:c.1333_1337delinsGAAAA (MSH6)	ENSP00000498629.1:p.Glu445=
ENST00000673637.1:c.1333_1337delinsGAAAA (MSH6)	ENSP00000501310.1:p.Glu445=
ENST00000234420.9:c.1630_1634delinsGAAAA (MSH6)	ENSP00000234420.4:p.Glu544=
ENST00000405808.5:c.169+8578_169+8582delinsTTTTC (FBXO11)	ENSP00000385127.1:n.169+8578_169+8582delinsTTTTC
ENST00000434234.5:c.*124+8377_*124+8381delinsTTTTC (FBXO11)	ENSP00000402692.1:n.*124+8377_*124+8381delinsTTTTC
ENST00000445503.5:c.*977_*981delinsGAAAA (MSH6)	ENSP00000405294.1:n.*977_*981delinsGAAAA
ENST00000538136.1:c.724_728delinsGAAAA (MSH6)	ENSP00000438580.1:p.Glu242=
ENST00000540021.5:c.1240_1244delinsGAAAA (MSH6)	ENSP00000446475.1:p.Glu414=
ENST00000614496.4:c.724_728delinsGAAAA (MSH6)	ENSP00000477844.1:p.Glu242=
ENST00000616033.4:c.1627_1631delinsGAAAA (MSH6)	ENSP00000480261.1:p.Glu543=
ENST00000622629.4:c.-1467_-1463delinsGAAAA (MSH6)	ENSP00000482078.1:n.-1467_-1463delinsGAAAA
NM_000179.2:c.1630_1634delinsGAAAA , LRG_219t1:c.1630_1634delinsGAAAA (MSH6)	NP_000170.1:p.Glu544=
NM_001281492.1:c.1240_1244delinsGAAAA (MSH6)	NP_001268421.1:p.Glu414=
NM_001281493.1:c.724_728delinsGAAAA (MSH6)	NP_001268422.1:p.Glu242=
NM_001281494.1:c.724_728delinsGAAAA (MSH6)	NP_001268423.1:p.Glu242=
XM_005264271.1:c.1333_1337delinsGAAAA (MSH6)	XP_005264328.1:p.Glu445=
XM_011532798.1:c.1447_1451delinsGAAAA (MSH6)	XP_011531100.1:p.Glu483=
XM_011532799.1:c.1333_1337delinsGAAAA (MSH6)	XP_011531101.1:p.Glu445=
XM_011532800.1:c.1333_1337delinsGAAAA (MSH6)	XP_011531102.1:p.Glu445=
XM_024452819.1:c.1630_1634delinsGAAAA (MSH6)	XP_024308587.1:p.Glu544=
XM_024452820.1:c.1447_1451delinsGAAAA (MSH6)	XP_024308588.1:p.Glu483=
XM_024452821.1:c.1333_1337delinsGAAAA (MSH6)	XP_024308589.1:p.Glu445=
XM_024452822.1:c.724_728delinsGAAAA (MSH6)	XP_024308590.1:p.Glu242=
NM_000179.3:c.1630_1634delinsGAAAA (MSH6) MANE Select	NP_000170.1:p.Glu544=
NM_001281492.2:c.1240_1244delinsGAAAA (MSH6)	NP_001268421.1:p.Glu414=
NM_001281493.2:c.724_728delinsGAAAA (MSH6)	NP_001268422.1:p.Glu242=
NM_001281494.2:c.724_728delinsGAAAA (MSH6)	NP_001268423.1:p.Glu242=