Canonical Allele Identifier: CA2496049212

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47800021_47800022delinsGC , CM000664.2:g.47800021_47800022delinsGC	GRCh38
NC_000002.11:g.48027160_48027161delinsGC , CM000664.1:g.48027160_48027161delinsGC	GRCh37
NC_000002.10:g.47880664_47880665delinsGC	NCBI36
NG_007111.1:g.21875_21876delinsGC , LRG_219:g.21875_21876delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.1741_1742delinsGC (MSH6)	ENSP00000406248.2:p.Ala581=
ENST00000420813.6:c.1741_1742delinsGC (MSH6)	ENSP00000390382.2:p.Ala581=
ENST00000455383.6:c.1741_1742delinsGC (MSH6)	ENSP00000397484.2:p.Ala581=
ENST00000700004.2:c.2038_2039delinsGC (MSH6)	ENSP00000514752.2:p.Ala680=
ENST00000699999.1:n.2122_2123delinsGC (MSH6)
ENST00000700000.1:c.1606+432_1606+433delinsGC (MSH6)	ENSP00000514749.1:n.1606+432_1606+433delinsGC
ENST00000700002.1:c.2044_2045delinsGC (MSH6)	ENSP00000514750.1:p.Ala682=
ENST00000700003.1:c.628-3399_628-3398delinsGC (MSH6)	ENSP00000514751.1:n.628-3399_628-3398delinsGC
ENST00000700004.1:c.1195_1196delinsGC (MSH6)	ENSP00000514752.1:p.Ala399=
ENST00000234420.11:c.2038_2039delinsGC (MSH6) MANE Select	ENSP00000234420.5:p.Ala680=
ENST00000540021.6:c.1648_1649delinsGC (MSH6)	ENSP00000446475.1:p.Ala550=
ENST00000652107.1:c.1741_1742delinsGC (MSH6)	ENSP00000498629.1:p.Ala581=
ENST00000673637.1:c.1741_1742delinsGC (MSH6)	ENSP00000501310.1:p.Ala581=
ENST00000234420.9:c.2038_2039delinsGC (MSH6)	ENSP00000234420.4:p.Ala680=
ENST00000405808.5:c.169+8173_169+8174delinsGC (FBXO11)	ENSP00000385127.1:n.169+8173_169+8174delinsGC
ENST00000434234.5:c.*124+7972_*124+7973delinsGC (FBXO11)	ENSP00000402692.1:n.*124+7972_*124+7973delinsGC
ENST00000445503.5:c.*1385_*1386delinsGC (MSH6)	ENSP00000405294.1:n.*1385_*1386delinsGC
ENST00000538136.1:c.1132_1133delinsGC (MSH6)	ENSP00000438580.1:p.Ala378=
ENST00000540021.5:c.1648_1649delinsGC (MSH6)	ENSP00000446475.1:p.Ala550=
ENST00000614496.4:c.1132_1133delinsGC (MSH6)	ENSP00000477844.1:p.Ala378=
ENST00000616033.4:c.2035_2036delinsGC (MSH6)	ENSP00000480261.1:p.Ala679=
ENST00000622629.4:c.-1059_-1058delinsGC (MSH6)	ENSP00000482078.1:n.-1059_-1058delinsGC
NM_000179.2:c.2038_2039delinsGC , LRG_219t1:c.2038_2039delinsGC (MSH6)	NP_000170.1:p.Ala680=
NM_001281492.1:c.1648_1649delinsGC (MSH6)	NP_001268421.1:p.Ala550=
NM_001281493.1:c.1132_1133delinsGC (MSH6)	NP_001268422.1:p.Ala378=
NM_001281494.1:c.1132_1133delinsGC (MSH6)	NP_001268423.1:p.Ala378=
XM_005264271.1:c.1741_1742delinsGC (MSH6)	XP_005264328.1:p.Ala581=
XM_011532798.1:c.1855_1856delinsGC (MSH6)	XP_011531100.1:p.Ala619=
XM_011532799.1:c.1741_1742delinsGC (MSH6)	XP_011531101.1:p.Ala581=
XM_011532800.1:c.1741_1742delinsGC (MSH6)	XP_011531102.1:p.Ala581=
XM_024452819.1:c.2038_2039delinsGC (MSH6)	XP_024308587.1:p.Ala680=
XM_024452820.1:c.1855_1856delinsGC (MSH6)	XP_024308588.1:p.Ala619=
XM_024452821.1:c.1741_1742delinsGC (MSH6)	XP_024308589.1:p.Ala581=
XM_024452822.1:c.1132_1133delinsGC (MSH6)	XP_024308590.1:p.Ala378=
NM_000179.3:c.2038_2039delinsGC (MSH6) MANE Select	NP_000170.1:p.Ala680=
NM_001281492.2:c.1648_1649delinsGC (MSH6)	NP_001268421.1:p.Ala550=
NM_001281493.2:c.1132_1133delinsGC (MSH6)	NP_001268422.1:p.Ala378=
NM_001281494.2:c.1132_1133delinsGC (MSH6)	NP_001268423.1:p.Ala378=