Canonical Allele Identifier: CA2496048942

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47799719_47799720delinsGT , CM000664.2:g.47799719_47799720delinsGT	GRCh38
NC_000002.11:g.48026858_48026859delinsGT , CM000664.1:g.48026858_48026859delinsGT	GRCh37
NC_000002.10:g.47880362_47880363delinsGT	NCBI36
NG_007111.1:g.21573_21574delinsGT , LRG_219:g.21573_21574delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.1439_1440delinsGT (MSH6)	ENSP00000406248.2:p.Cys480=
ENST00000420813.6:c.1439_1440delinsGT (MSH6)	ENSP00000390382.2:p.Cys480=
ENST00000455383.6:c.1439_1440delinsGT (MSH6)	ENSP00000397484.2:p.Cys480=
ENST00000700004.2:c.1736_1737delinsGT (MSH6)	ENSP00000514752.2:p.Cys579=
ENST00000699999.1:n.1820_1821delinsGT (MSH6)
ENST00000700000.1:c.1606+130_1606+131delinsGT (MSH6)	ENSP00000514749.1:n.1606+130_1606+131delinsGT
ENST00000700002.1:c.1742_1743delinsGT (MSH6)	ENSP00000514750.1:p.Cys581=
ENST00000700003.1:c.627+3656_627+3657delinsGT (MSH6)	ENSP00000514751.1:n.627+3656_627+3657delinsGT
ENST00000700004.1:c.893_894delinsGT (MSH6)	ENSP00000514752.1:p.Cys298=
ENST00000234420.11:c.1736_1737delinsGT (MSH6) MANE Select	ENSP00000234420.5:p.Cys579=
ENST00000540021.6:c.1346_1347delinsGT (MSH6)	ENSP00000446475.1:p.Cys449=
ENST00000652107.1:c.1439_1440delinsGT (MSH6)	ENSP00000498629.1:p.Cys480=
ENST00000673637.1:c.1439_1440delinsGT (MSH6)	ENSP00000501310.1:p.Cys480=
ENST00000234420.9:c.1736_1737delinsGT (MSH6)	ENSP00000234420.4:p.Cys579=
ENST00000405808.5:c.169+8475_169+8476delinsAC (FBXO11)	ENSP00000385127.1:n.169+8475_169+8476delinsAC
ENST00000434234.5:c.*124+8274_*124+8275delinsAC (FBXO11)	ENSP00000402692.1:n.*124+8274_*124+8275delinsAC
ENST00000445503.5:c.*1083_*1084delinsGT (MSH6)	ENSP00000405294.1:n.*1083_*1084delinsGT
ENST00000538136.1:c.830_831delinsGT (MSH6)	ENSP00000438580.1:p.Cys277=
ENST00000540021.5:c.1346_1347delinsGT (MSH6)	ENSP00000446475.1:p.Cys449=
ENST00000614496.4:c.830_831delinsGT (MSH6)	ENSP00000477844.1:p.Cys277=
ENST00000616033.4:c.1733_1734delinsGT (MSH6)	ENSP00000480261.1:p.Cys578=
ENST00000622629.4:c.-1361_-1360delinsGT (MSH6)	ENSP00000482078.1:n.-1361_-1360delinsGT
NM_000179.2:c.1736_1737delinsGT , LRG_219t1:c.1736_1737delinsGT (MSH6)	NP_000170.1:p.Cys579=
NM_001281492.1:c.1346_1347delinsGT (MSH6)	NP_001268421.1:p.Cys449=
NM_001281493.1:c.830_831delinsGT (MSH6)	NP_001268422.1:p.Cys277=
NM_001281494.1:c.830_831delinsGT (MSH6)	NP_001268423.1:p.Cys277=
XM_005264271.1:c.1439_1440delinsGT (MSH6)	XP_005264328.1:p.Cys480=
XM_011532798.1:c.1553_1554delinsGT (MSH6)	XP_011531100.1:p.Cys518=
XM_011532799.1:c.1439_1440delinsGT (MSH6)	XP_011531101.1:p.Cys480=
XM_011532800.1:c.1439_1440delinsGT (MSH6)	XP_011531102.1:p.Cys480=
XM_024452819.1:c.1736_1737delinsGT (MSH6)	XP_024308587.1:p.Cys579=
XM_024452820.1:c.1553_1554delinsGT (MSH6)	XP_024308588.1:p.Cys518=
XM_024452821.1:c.1439_1440delinsGT (MSH6)	XP_024308589.1:p.Cys480=
XM_024452822.1:c.830_831delinsGT (MSH6)	XP_024308590.1:p.Cys277=
NM_000179.3:c.1736_1737delinsGT (MSH6) MANE Select	NP_000170.1:p.Cys579=
NM_001281492.2:c.1346_1347delinsGT (MSH6)	NP_001268421.1:p.Cys449=
NM_001281493.2:c.830_831delinsGT (MSH6)	NP_001268422.1:p.Cys277=
NM_001281494.2:c.830_831delinsGT (MSH6)	NP_001268423.1:p.Cys277=