Canonical Allele Identifier: CA46720309

Gene: MSH6 FBXO11

Linked Data

• MyVariant Identifiers: chr2:g.48033909_48033910insAA (hg19) ; chr2:g.47806770_47806771insAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806770_47806771dup , CM000664.2:g.47806770_47806771dup	GRCh38
NC_000002.11:g.48033909_48033910dup , CM000664.1:g.48033909_48033910dup	GRCh37
NC_000002.10:g.47887413_47887414dup	NCBI36
NG_007111.1:g.28624_28625dup , LRG_219:g.28624_28625dup
NG_008397.1:g.103905_103906dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3705-9_3705-8dup (MSH6)	ENSP00000406248.2:n.3705-9_3705-8dup
ENST00000420813.6:c.3705-9_3705-8dup (MSH6)	ENSP00000390382.2:n.3705-9_3705-8dup
ENST00000455383.6:c.3705-9_3705-8dup (MSH6)	ENSP00000397484.2:n.3705-9_3705-8dup
ENST00000700004.2:c.3618-9_3618-8dup (MSH6)	ENSP00000514752.2:n.3618-9_3618-8dup
ENST00000699999.1:n.4676-9_4676-8dup (MSH6)
ENST00000700000.1:c.2436-9_2436-8dup (MSH6)	ENSP00000514749.1:n.2436-9_2436-8dup
ENST00000700002.1:c.4008-9_4008-8dup (MSH6)	ENSP00000514750.1:n.4008-9_4008-8dup
ENST00000700003.1:c.1457-9_1457-8dup (MSH6)	ENSP00000514751.1:n.1457-9_1457-8dup
ENST00000700004.1:c.2775-9_2775-8dup (MSH6)	ENSP00000514752.1:n.2775-9_2775-8dup
ENST00000700005.1:n.2971_2972dup (MSH6)
ENST00000700007.1:n.2597-9_2597-8dup (MSH6)
ENST00000700008.1:n.2264-9_2264-8dup (MSH6)
ENST00000700009.1:n.2666-9_2666-8dup (MSH6)
ENST00000700010.1:n.1411-9_1411-8dup (MSH6)
ENST00000700011.1:n.3296-9_3296-8dup (MSH6)
ENST00000682451.1:n.3977_3978dup (FBXO11)
ENST00000684712.1:n.4239_4240dup (FBXO11)
ENST00000234420.11:c.4002-9_4002-8dup (MSH6) MANE Select	ENSP00000234420.5:n.4002-9_4002-8dup
ENST00000540021.6:c.3612-9_3612-8dup (MSH6)	ENSP00000446475.1:n.3612-9_3612-8dup
ENST00000652107.1:c.3705-9_3705-8dup (MSH6)	ENSP00000498629.1:n.3705-9_3705-8dup
ENST00000673637.1:c.3705-9_3705-8dup (MSH6)	ENSP00000501310.1:n.3705-9_3705-8dup
ENST00000234420.9:c.4002-9_4002-8dup (MSH6)	ENSP00000234420.4:n.4002-9_4002-8dup
ENST00000405808.5:c.169+1424_169+1425dup (FBXO11)	ENSP00000385127.1:n.169+1424_169+1425dup
ENST00000434234.5:c.*124+1223_*124+1224dup (FBXO11)	ENSP00000402692.1:n.*124+1223_*124+1224dup
ENST00000445503.5:c.*3349-9_*3349-8dup (MSH6)	ENSP00000405294.1:n.*3349-9_*3349-8dup
ENST00000465204.5:n.3139_3140dup (FBXO11)
ENST00000538136.1:c.3096-9_3096-8dup (MSH6)	ENSP00000438580.1:n.3096-9_3096-8dup
ENST00000540021.5:c.3612-9_3612-8dup (MSH6)	ENSP00000446475.1:n.3612-9_3612-8dup
ENST00000614496.4:c.3096-9_3096-8dup (MSH6)	ENSP00000477844.1:n.3096-9_3096-8dup
ENST00000622629.4:c.903-9_903-8dup (MSH6)	ENSP00000482078.1:n.903-9_903-8dup
NM_000179.2:c.4002-9_4002-8dup , LRG_219t1:c.4002-9_4002-8dup (MSH6)	NP_000170.1:n.4002-9_4002-8dup
NM_001281492.1:c.3612-9_3612-8dup (MSH6)	NP_001268421.1:n.3612-9_3612-8dup
NM_001281493.1:c.3096-9_3096-8dup (MSH6)	NP_001268422.1:n.3096-9_3096-8dup
NM_001281494.1:c.3096-9_3096-8dup (MSH6)	NP_001268423.1:n.3096-9_3096-8dup
XM_005264271.1:c.3705-9_3705-8dup (MSH6)	XP_005264328.1:n.3705-9_3705-8dup
XM_011532798.1:c.3819-9_3819-8dup (MSH6)	XP_011531100.1:n.3819-9_3819-8dup
XM_011532799.1:c.3705-9_3705-8dup (MSH6)	XP_011531101.1:n.3705-9_3705-8dup
XM_011532800.1:c.3705-9_3705-8dup (MSH6)	XP_011531102.1:n.3705-9_3705-8dup
XM_024452819.1:c.4095-9_4095-8dup (MSH6)	XP_024308587.1:n.4095-9_4095-8dup
XM_024452820.1:c.3912-9_3912-8dup (MSH6)	XP_024308588.1:n.3912-9_3912-8dup
XM_024452821.1:c.3798-9_3798-8dup (MSH6)	XP_024308589.1:n.3798-9_3798-8dup
XM_024452822.1:c.3189-9_3189-8dup (MSH6)	XP_024308590.1:n.3189-9_3189-8dup
NM_000179.3:c.4002-9_4002-8dup (MSH6) MANE Select	NP_000170.1:n.4002-9_4002-8dup
NM_001281492.2:c.3612-9_3612-8dup (MSH6)	NP_001268421.1:n.3612-9_3612-8dup
NM_001281493.2:c.3096-9_3096-8dup (MSH6)	NP_001268422.1:n.3096-9_3096-8dup
NM_001281494.2:c.3096-9_3096-8dup (MSH6)	NP_001268423.1:n.3096-9_3096-8dup