Canonical Allele Identifier: CA2496049973

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47800926_47800927delinsTC , CM000664.2:g.47800926_47800927delinsTC	GRCh38
NC_000002.11:g.48028065_48028066delinsTC , CM000664.1:g.48028065_48028066delinsTC	GRCh37
NC_000002.10:g.47881569_47881570delinsTC	NCBI36
NG_007111.1:g.22780_22781delinsTC , LRG_219:g.22780_22781delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.2646_2647delinsTC (MSH6)	ENSP00000406248.2:p.Ile882=
ENST00000420813.6:c.2646_2647delinsTC (MSH6)	ENSP00000390382.2:p.Ile882=
ENST00000455383.6:c.2646_2647delinsTC (MSH6)	ENSP00000397484.2:p.Ile882=
ENST00000700004.2:c.2943_2944delinsTC (MSH6)	ENSP00000514752.2:p.Ile981=
ENST00000699999.1:n.3027_3028delinsTC (MSH6)
ENST00000700000.1:c.1606+1337_1606+1338delinsTC (MSH6)	ENSP00000514749.1:n.1606+1337_1606+1338delinsTC
ENST00000700002.1:c.2949_2950delinsTC (MSH6)	ENSP00000514750.1:p.Ile983=
ENST00000700003.1:c.628-2494_628-2493delinsTC (MSH6)	ENSP00000514751.1:n.628-2494_628-2493delinsTC
ENST00000700004.1:c.2100_2101delinsTC (MSH6)	ENSP00000514752.1:p.Ile700=
ENST00000234420.11:c.2943_2944delinsTC (MSH6) MANE Select	ENSP00000234420.5:p.Ile981=
ENST00000540021.6:c.2553_2554delinsTC (MSH6)	ENSP00000446475.1:p.Ile851=
ENST00000652107.1:c.2646_2647delinsTC (MSH6)	ENSP00000498629.1:p.Ile882=
ENST00000673637.1:c.2646_2647delinsTC (MSH6)	ENSP00000501310.1:p.Ile882=
ENST00000234420.9:c.2943_2944delinsTC (MSH6)	ENSP00000234420.4:p.Ile981=
ENST00000405808.5:c.169+7268_169+7269delinsGA (FBXO11)	ENSP00000385127.1:n.169+7268_169+7269delinsGA
ENST00000434234.5:c.*124+7067_*124+7068delinsGA (FBXO11)	ENSP00000402692.1:n.*124+7067_*124+7068delinsGA
ENST00000445503.5:c.*2290_*2291delinsTC (MSH6)	ENSP00000405294.1:n.*2290_*2291delinsTC
ENST00000538136.1:c.2037_2038delinsTC (MSH6)	ENSP00000438580.1:p.Ile679=
ENST00000540021.5:c.2553_2554delinsTC (MSH6)	ENSP00000446475.1:p.Ile851=
ENST00000614496.4:c.2037_2038delinsTC (MSH6)	ENSP00000477844.1:p.Ile679=
ENST00000616033.4:c.2940_2941delinsTC (MSH6)	ENSP00000480261.1:p.Ile980=
ENST00000622629.4:c.-154_-153delinsTC (MSH6)	ENSP00000482078.1:n.-154_-153delinsTC
NM_000179.2:c.2943_2944delinsTC , LRG_219t1:c.2943_2944delinsTC (MSH6)	NP_000170.1:p.Ile981=
NM_001281492.1:c.2553_2554delinsTC (MSH6)	NP_001268421.1:p.Ile851=
NM_001281493.1:c.2037_2038delinsTC (MSH6)	NP_001268422.1:p.Ile679=
NM_001281494.1:c.2037_2038delinsTC (MSH6)	NP_001268423.1:p.Ile679=
XM_005264271.1:c.2646_2647delinsTC (MSH6)	XP_005264328.1:p.Ile882=
XM_011532798.1:c.2760_2761delinsTC (MSH6)	XP_011531100.1:p.Ile920=
XM_011532799.1:c.2646_2647delinsTC (MSH6)	XP_011531101.1:p.Ile882=
XM_011532800.1:c.2646_2647delinsTC (MSH6)	XP_011531102.1:p.Ile882=
XM_024452819.1:c.2943_2944delinsTC (MSH6)	XP_024308587.1:p.Ile981=
XM_024452820.1:c.2760_2761delinsTC (MSH6)	XP_024308588.1:p.Ile920=
XM_024452821.1:c.2646_2647delinsTC (MSH6)	XP_024308589.1:p.Ile882=
XM_024452822.1:c.2037_2038delinsTC (MSH6)	XP_024308590.1:p.Ile679=
NM_000179.3:c.2943_2944delinsTC (MSH6) MANE Select	NP_000170.1:p.Ile981=
NM_001281492.2:c.2553_2554delinsTC (MSH6)	NP_001268421.1:p.Ile851=
NM_001281493.2:c.2037_2038delinsTC (MSH6)	NP_001268422.1:p.Ile679=
NM_001281494.2:c.2037_2038delinsTC (MSH6)	NP_001268423.1:p.Ile679=