Canonical Allele Identifier: CA2496049636

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47800544_47800545delinsAG , CM000664.2:g.47800544_47800545delinsAG	GRCh38
NC_000002.11:g.48027683_48027684delinsAG , CM000664.1:g.48027683_48027684delinsAG	GRCh37
NC_000002.10:g.47881187_47881188delinsAG	NCBI36
NG_007111.1:g.22398_22399delinsAG , LRG_219:g.22398_22399delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.2264_2265delinsAG (MSH6)	ENSP00000406248.2:p.Lys755=
ENST00000420813.6:c.2264_2265delinsAG (MSH6)	ENSP00000390382.2:p.Lys755=
ENST00000455383.6:c.2264_2265delinsAG (MSH6)	ENSP00000397484.2:p.Lys755=
ENST00000700004.2:c.2561_2562delinsAG (MSH6)	ENSP00000514752.2:p.Lys854=
ENST00000699999.1:n.2645_2646delinsAG (MSH6)
ENST00000700000.1:c.1606+955_1606+956delinsAG (MSH6)	ENSP00000514749.1:n.1606+955_1606+956deli...
ENST00000700002.1:c.2567_2568delinsAG (MSH6)	ENSP00000514750.1:p.Lys856=
ENST00000700003.1:c.628-2876_628-2875delinsAG (MSH6)	ENSP00000514751.1:n.628-2876_628-2875deli...
ENST00000700004.1:c.1718_1719delinsAG (MSH6)	ENSP00000514752.1:p.Lys573=
ENST00000234420.11:c.2561_2562delinsAG (MSH6) MANE Select	ENSP00000234420.5:p.Lys854=
ENST00000540021.6:c.2171_2172delinsAG (MSH6)	ENSP00000446475.1:p.Lys724=
ENST00000652107.1:c.2264_2265delinsAG (MSH6)	ENSP00000498629.1:p.Lys755=
ENST00000673637.1:c.2264_2265delinsAG (MSH6)	ENSP00000501310.1:p.Lys755=
ENST00000234420.9:c.2561_2562delinsAG (MSH6)	ENSP00000234420.4:p.Lys854=
ENST00000405808.5:c.169+7650_169+7651delinsCT (FBXO11)	ENSP00000385127.1:n.169+7650_169+7651deli...
ENST00000434234.5:c.*124+7449_*124+7450delinsCT (FBXO11)	ENSP00000402692.1:n.*124+7449_*124+7450de...
ENST00000445503.5:c.*1908_*1909delinsAG (MSH6)	ENSP00000405294.1:n.*1908_*1909delinsAG
ENST00000538136.1:c.1655_1656delinsAG (MSH6)	ENSP00000438580.1:p.Lys552=
ENST00000540021.5:c.2171_2172delinsAG (MSH6)	ENSP00000446475.1:p.Lys724=
ENST00000614496.4:c.1655_1656delinsAG (MSH6)	ENSP00000477844.1:p.Lys552=
ENST00000616033.4:c.2558_2559delinsAG (MSH6)	ENSP00000480261.1:p.Lys853=
ENST00000622629.4:c.-536_-535delinsAG (MSH6)	ENSP00000482078.1:n.-536_-535delinsAG
NM_000179.2:c.2561_2562delinsAG , LRG_219t1:c.2561_2562delinsAG (MSH6)	NP_000170.1:p.Lys854=
NM_001281492.1:c.2171_2172delinsAG (MSH6)	NP_001268421.1:p.Lys724=
NM_001281493.1:c.1655_1656delinsAG (MSH6)	NP_001268422.1:p.Lys552=
NM_001281494.1:c.1655_1656delinsAG (MSH6)	NP_001268423.1:p.Lys552=
XM_005264271.1:c.2264_2265delinsAG (MSH6)	XP_005264328.1:p.Lys755=
XM_011532798.1:c.2378_2379delinsAG (MSH6)	XP_011531100.1:p.Lys793=
XM_011532799.1:c.2264_2265delinsAG (MSH6)	XP_011531101.1:p.Lys755=
XM_011532800.1:c.2264_2265delinsAG (MSH6)	XP_011531102.1:p.Lys755=
XM_024452819.1:c.2561_2562delinsAG (MSH6)	XP_024308587.1:p.Lys854=
XM_024452820.1:c.2378_2379delinsAG (MSH6)	XP_024308588.1:p.Lys793=
XM_024452821.1:c.2264_2265delinsAG (MSH6)	XP_024308589.1:p.Lys755=
XM_024452822.1:c.1655_1656delinsAG (MSH6)	XP_024308590.1:p.Lys552=
NM_000179.3:c.2561_2562delinsAG (MSH6) MANE Select	NP_000170.1:p.Lys854=
NM_001281492.2:c.2171_2172delinsAG (MSH6)	NP_001268421.1:p.Lys724=
NM_001281493.2:c.1655_1656delinsAG (MSH6)	NP_001268422.1:p.Lys552=
NM_001281494.2:c.1655_1656delinsAG (MSH6)	NP_001268423.1:p.Lys552=