Canonical Allele Identifier: CA2496049225

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47800032_47800033delinsTC , CM000664.2:g.47800032_47800033delinsTC	GRCh38
NC_000002.11:g.48027171_48027172delinsTC , CM000664.1:g.48027171_48027172delinsTC	GRCh37
NC_000002.10:g.47880675_47880676delinsTC	NCBI36
NG_007111.1:g.21886_21887delinsTC , LRG_219:g.21886_21887delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.1752_1753delinsTC (MSH6)	ENSP00000406248.2:p.Ala584=
ENST00000420813.6:c.1752_1753delinsTC (MSH6)	ENSP00000390382.2:p.Ala584=
ENST00000455383.6:c.1752_1753delinsTC (MSH6)	ENSP00000397484.2:p.Ala584=
ENST00000700004.2:c.2049_2050delinsTC (MSH6)	ENSP00000514752.2:p.Ala683=
ENST00000699999.1:n.2133_2134delinsTC (MSH6)
ENST00000700000.1:c.1606+443_1606+444delinsTC (MSH6)	ENSP00000514749.1:n.1606+443_1606+444delinsTC
ENST00000700002.1:c.2055_2056delinsTC (MSH6)	ENSP00000514750.1:p.Ala685=
ENST00000700003.1:c.628-3388_628-3387delinsTC (MSH6)	ENSP00000514751.1:n.628-3388_628-3387delinsTC
ENST00000700004.1:c.1206_1207delinsTC (MSH6)	ENSP00000514752.1:p.Ala402=
ENST00000234420.11:c.2049_2050delinsTC (MSH6) MANE Select	ENSP00000234420.5:p.Ala683=
ENST00000540021.6:c.1659_1660delinsTC (MSH6)	ENSP00000446475.1:p.Ala553=
ENST00000652107.1:c.1752_1753delinsTC (MSH6)	ENSP00000498629.1:p.Ala584=
ENST00000673637.1:c.1752_1753delinsTC (MSH6)	ENSP00000501310.1:p.Ala584=
ENST00000234420.9:c.2049_2050delinsTC (MSH6)	ENSP00000234420.4:p.Ala683=
ENST00000405808.5:c.169+8162_169+8163delinsGA (FBXO11)	ENSP00000385127.1:n.169+8162_169+8163delinsGA
ENST00000434234.5:c.*124+7961_*124+7962delinsGA (FBXO11)	ENSP00000402692.1:n.*124+7961_*124+7962delinsGA
ENST00000445503.5:c.*1396_*1397delinsTC (MSH6)	ENSP00000405294.1:n.*1396_*1397delinsTC
ENST00000538136.1:c.1143_1144delinsTC (MSH6)	ENSP00000438580.1:p.Ala381=
ENST00000540021.5:c.1659_1660delinsTC (MSH6)	ENSP00000446475.1:p.Ala553=
ENST00000614496.4:c.1143_1144delinsTC (MSH6)	ENSP00000477844.1:p.Ala381=
ENST00000616033.4:c.2046_2047delinsTC (MSH6)	ENSP00000480261.1:p.Ala682=
ENST00000622629.4:c.-1048_-1047delinsTC (MSH6)	ENSP00000482078.1:n.-1048_-1047delinsTC
NM_000179.2:c.2049_2050delinsTC , LRG_219t1:c.2049_2050delinsTC (MSH6)	NP_000170.1:p.Ala683=
NM_001281492.1:c.1659_1660delinsTC (MSH6)	NP_001268421.1:p.Ala553=
NM_001281493.1:c.1143_1144delinsTC (MSH6)	NP_001268422.1:p.Ala381=
NM_001281494.1:c.1143_1144delinsTC (MSH6)	NP_001268423.1:p.Ala381=
XM_005264271.1:c.1752_1753delinsTC (MSH6)	XP_005264328.1:p.Ala584=
XM_011532798.1:c.1866_1867delinsTC (MSH6)	XP_011531100.1:p.Ala622=
XM_011532799.1:c.1752_1753delinsTC (MSH6)	XP_011531101.1:p.Ala584=
XM_011532800.1:c.1752_1753delinsTC (MSH6)	XP_011531102.1:p.Ala584=
XM_024452819.1:c.2049_2050delinsTC (MSH6)	XP_024308587.1:p.Ala683=
XM_024452820.1:c.1866_1867delinsTC (MSH6)	XP_024308588.1:p.Ala622=
XM_024452821.1:c.1752_1753delinsTC (MSH6)	XP_024308589.1:p.Ala584=
XM_024452822.1:c.1143_1144delinsTC (MSH6)	XP_024308590.1:p.Ala381=
NM_000179.3:c.2049_2050delinsTC (MSH6) MANE Select	NP_000170.1:p.Ala683=
NM_001281492.2:c.1659_1660delinsTC (MSH6)	NP_001268421.1:p.Ala553=
NM_001281493.2:c.1143_1144delinsTC (MSH6)	NP_001268422.1:p.Ala381=
NM_001281494.2:c.1143_1144delinsTC (MSH6)	NP_001268423.1:p.Ala381=