Canonical Allele Identifier: CA2496053992

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806211_47806215delinsTACTG , CM000664.2:g.47806211_47806215delinsTACTG	GRCh38
NC_000002.11:g.48033350_48033354delinsTACTG , CM000664.1:g.48033350_48033354delinsTACTG	GRCh37
NC_000002.10:g.47886854_47886858delinsTACTG	NCBI36
NG_007111.1:g.28065_28069delinsTACTG , LRG_219:g.28065_28069delinsTACTG
NG_008397.1:g.104461_104465delinsCAGTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3357_3361delinsTACTG (MSH6)	ENSP00000406248.2:p.Gly1119=
ENST00000420813.6:c.3357_3361delinsTACTG (MSH6)	ENSP00000390382.2:p.Gly1119=
ENST00000455383.6:c.3357_3361delinsTACTG (MSH6)	ENSP00000397484.2:p.Gly1119=
ENST00000700004.2:c.3270_3274delinsTACTG (MSH6)	ENSP00000514752.2:p.Gly1090=
ENST00000699999.1:n.4328_4332delinsTACTG (MSH6)
ENST00000700000.1:c.2088_2092delinsTACTG (MSH6)	ENSP00000514749.1:p.Gly696=
ENST00000700002.1:c.3660_3664delinsTACTG (MSH6)	ENSP00000514750.1:p.Gly1220=
ENST00000700003.1:c.1109_1113delinsTACTG (MSH6)	ENSP00000514751.1:n.1109_1113delinsTACTG
ENST00000700004.1:c.2427_2431delinsTACTG (MSH6)	ENSP00000514752.1:p.Gly809=
ENST00000700005.1:n.2505_2509delinsTACTG (MSH6)
ENST00000700006.1:n.4812_4816delinsTACTG (MSH6)
ENST00000700007.1:n.2249_2253delinsTACTG (MSH6)
ENST00000700008.1:n.1823_1827delinsTACTG (MSH6)
ENST00000700009.1:n.2318_2322delinsTACTG (MSH6)
ENST00000700010.1:n.1063_1067delinsTACTG (MSH6)
ENST00000700011.1:n.2948_2952delinsTACTG (MSH6)
ENST00000682451.1:n.4533_4537delinsCAGTA (FBXO11)
ENST00000684712.1:n.4795_4799delinsCAGTA (FBXO11)
ENST00000234420.11:c.3654_3658delinsTACTG (MSH6) MANE Select	ENSP00000234420.5:p.Gly1218=
ENST00000540021.6:c.3264_3268delinsTACTG (MSH6)	ENSP00000446475.1:p.Gly1088=
ENST00000652107.1:c.3357_3361delinsTACTG (MSH6)	ENSP00000498629.1:p.Gly1119=
ENST00000673637.1:c.3357_3361delinsTACTG (MSH6)	ENSP00000501310.1:p.Gly1119=
ENST00000234420.9:c.3654_3658delinsTACTG (MSH6)	ENSP00000234420.4:p.Gly1218=
ENST00000405808.5:c.169+1980_169+1984delinsCAGTA (FBXO11)	ENSP00000385127.1:n.169+1980_169+1984delinsCAGTA
ENST00000434234.5:c.*124+1779_*124+1783delinsCAGTA (FBXO11)	ENSP00000402692.1:n.*124+1779_*124+1783delinsCAGTA
ENST00000445503.5:c.*3001_*3005delinsTACTG (MSH6)	ENSP00000405294.1:n.*3001_*3005delinsTACTG
ENST00000538136.1:c.2748_2752delinsTACTG (MSH6)	ENSP00000438580.1:p.Gly916=
ENST00000540021.5:c.3264_3268delinsTACTG (MSH6)	ENSP00000446475.1:p.Gly1088=
ENST00000614496.4:c.2748_2752delinsTACTG (MSH6)	ENSP00000477844.1:p.Gly916=
ENST00000622629.4:c.558_562delinsTACTG (MSH6)	ENSP00000482078.1:p.Gly186=
NM_000179.2:c.3654_3658delinsTACTG , LRG_219t1:c.3654_3658delinsTACTG (MSH6)	NP_000170.1:p.Gly1218=
NM_001281492.1:c.3264_3268delinsTACTG (MSH6)	NP_001268421.1:p.Gly1088=
NM_001281493.1:c.2748_2752delinsTACTG (MSH6)	NP_001268422.1:p.Gly916=
NM_001281494.1:c.2748_2752delinsTACTG (MSH6)	NP_001268423.1:p.Gly916=
XM_005264271.1:c.3357_3361delinsTACTG (MSH6)	XP_005264328.1:p.Gly1119=
XM_011532798.1:c.3471_3475delinsTACTG (MSH6)	XP_011531100.1:p.Gly1157=
XM_011532799.1:c.3357_3361delinsTACTG (MSH6)	XP_011531101.1:p.Gly1119=
XM_011532800.1:c.3357_3361delinsTACTG (MSH6)	XP_011531102.1:p.Gly1119=
XM_024452819.1:c.3654_3658delinsTACTG (MSH6)	XP_024308587.1:p.Gly1218=
XM_024452820.1:c.3471_3475delinsTACTG (MSH6)	XP_024308588.1:p.Gly1157=
XM_024452821.1:c.3357_3361delinsTACTG (MSH6)	XP_024308589.1:p.Gly1119=
XM_024452822.1:c.2748_2752delinsTACTG (MSH6)	XP_024308590.1:p.Gly916=
NM_000179.3:c.3654_3658delinsTACTG (MSH6) MANE Select	NP_000170.1:p.Gly1218=
NM_001281492.2:c.3264_3268delinsTACTG (MSH6)	NP_001268421.1:p.Gly1088=
NM_001281493.2:c.2748_2752delinsTACTG (MSH6)	NP_001268422.1:p.Gly916=
NM_001281494.2:c.2748_2752delinsTACTG (MSH6)	NP_001268423.1:p.Gly916=