Canonical Allele Identifier: CA2658969849

Gene: MSH6 FBXO11

Linked Data

• gnomAD v4: 2-47806751-C-CTTCTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806753_47806754insCTTTTTT , CM000664.2:g.47806753_47806754insCTTTTTT	GRCh38
NC_000002.11:g.48033892_48033893insCTTTTTT , CM000664.1:g.48033892_48033893insCTTTTTT	GRCh37
NC_000002.10:g.47887396_47887397insCTTTTTT	NCBI36
NG_007111.1:g.28607_28608insCTTTTTT , LRG_219:g.28607_28608insCTTTTTT
NG_008397.1:g.103924_103925insAAAAGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3705-26_3705-25insCTTTTTT (MSH6)	ENSP00000406248.2:n.3705-26_3705-25insCTTTTTT
ENST00000420813.6:c.3705-26_3705-25insCTTTTTT (MSH6)	ENSP00000390382.2:n.3705-26_3705-25insCTTTTTT
ENST00000455383.6:c.3705-26_3705-25insCTTTTTT (MSH6)	ENSP00000397484.2:n.3705-26_3705-25insCTTTTTT
ENST00000700004.2:c.3618-26_3618-25insCTTTTTT (MSH6)	ENSP00000514752.2:n.3618-26_3618-25insCTTTTTT
ENST00000699999.1:n.4676-26_4676-25insCTTTTTT (MSH6)
ENST00000700000.1:c.2436-26_2436-25insCTTTTTT (MSH6)	ENSP00000514749.1:n.2436-26_2436-25insCTTTTTT
ENST00000700002.1:c.4008-26_4008-25insCTTTTTT (MSH6)	ENSP00000514750.1:n.4008-26_4008-25insCTTTTTT
ENST00000700003.1:c.1457-26_1457-25insCTTTTTT (MSH6)	ENSP00000514751.1:n.1457-26_1457-25insCTTTTTT
ENST00000700004.1:c.2775-26_2775-25insCTTTTTT (MSH6)	ENSP00000514752.1:n.2775-26_2775-25insCTTTTTT
ENST00000700005.1:n.2954_2955insCTTTTTT (MSH6)
ENST00000700007.1:n.2597-26_2597-25insCTTTTTT (MSH6)
ENST00000700008.1:n.2264-26_2264-25insCTTTTTT (MSH6)
ENST00000700009.1:n.2666-26_2666-25insCTTTTTT (MSH6)
ENST00000700010.1:n.1411-26_1411-25insCTTTTTT (MSH6)
ENST00000700011.1:n.3296-26_3296-25insCTTTTTT (MSH6)
ENST00000682451.1:n.3996_3997insAAAAGAA (FBXO11)
ENST00000684712.1:n.4258_4259insAAAAGAA (FBXO11)
ENST00000234420.11:c.4002-26_4002-25insCTTTTTT (MSH6) MANE Select	ENSP00000234420.5:n.4002-26_4002-25insCTTTTTT
ENST00000540021.6:c.3612-26_3612-25insCTTTTTT (MSH6)	ENSP00000446475.1:n.3612-26_3612-25insCTTTTTT
ENST00000652107.1:c.3705-26_3705-25insCTTTTTT (MSH6)	ENSP00000498629.1:n.3705-26_3705-25insCTTTTTT
ENST00000673637.1:c.3705-26_3705-25insCTTTTTT (MSH6)	ENSP00000501310.1:n.3705-26_3705-25insCTTTTTT
ENST00000234420.9:c.4002-26_4002-25insCTTTTTT (MSH6)	ENSP00000234420.4:n.4002-26_4002-25insCTTTTTT
ENST00000405808.5:c.169+1443_169+1444insAAAAGAA (FBXO11)	ENSP00000385127.1:n.169+1443_169+1444insAAAAGAA
ENST00000434234.5:c.*124+1242_*124+1243insAAAAGAA (FBXO11)	ENSP00000402692.1:n.*124+1242_*124+1243insAAAAGAA
ENST00000445503.5:c.*3349-26_*3349-25insCTTTTTT (MSH6)	ENSP00000405294.1:n.*3349-26_*3349-25insCTTTTTT
ENST00000538136.1:c.3096-26_3096-25insCTTTTTT (MSH6)	ENSP00000438580.1:n.3096-26_3096-25insCTTTTTT
ENST00000540021.5:c.3612-26_3612-25insCTTTTTT (MSH6)	ENSP00000446475.1:n.3612-26_3612-25insCTTTTTT
ENST00000614496.4:c.3096-26_3096-25insCTTTTTT (MSH6)	ENSP00000477844.1:n.3096-26_3096-25insCTTTTTT
ENST00000622629.4:c.903-26_903-25insCTTTTTT (MSH6)	ENSP00000482078.1:n.903-26_903-25insCTTTTTT
NM_000179.2:c.4002-26_4002-25insCTTTTTT , LRG_219t1:c.4002-26_4002-25insCTTTTTT (MSH6)	NP_000170.1:n.4002-26_4002-25insCTTTTTT
NM_001281492.1:c.3612-26_3612-25insCTTTTTT (MSH6)	NP_001268421.1:n.3612-26_3612-25insCTTTTTT
NM_001281493.1:c.3096-26_3096-25insCTTTTTT (MSH6)	NP_001268422.1:n.3096-26_3096-25insCTTTTTT
NM_001281494.1:c.3096-26_3096-25insCTTTTTT (MSH6)	NP_001268423.1:n.3096-26_3096-25insCTTTTTT
XM_005264271.1:c.3705-26_3705-25insCTTTTTT (MSH6)	XP_005264328.1:n.3705-26_3705-25insCTTTTTT
XM_011532798.1:c.3819-26_3819-25insCTTTTTT (MSH6)	XP_011531100.1:n.3819-26_3819-25insCTTTTTT
XM_011532799.1:c.3705-26_3705-25insCTTTTTT (MSH6)	XP_011531101.1:n.3705-26_3705-25insCTTTTTT
XM_011532800.1:c.3705-26_3705-25insCTTTTTT (MSH6)	XP_011531102.1:n.3705-26_3705-25insCTTTTTT
XM_024452819.1:c.4095-26_4095-25insCTTTTTT (MSH6)	XP_024308587.1:n.4095-26_4095-25insCTTTTTT
XM_024452820.1:c.3912-26_3912-25insCTTTTTT (MSH6)	XP_024308588.1:n.3912-26_3912-25insCTTTTTT
XM_024452821.1:c.3798-26_3798-25insCTTTTTT (MSH6)	XP_024308589.1:n.3798-26_3798-25insCTTTTTT
XM_024452822.1:c.3189-26_3189-25insCTTTTTT (MSH6)	XP_024308590.1:n.3189-26_3189-25insCTTTTTT
NM_000179.3:c.4002-26_4002-25insCTTTTTT (MSH6) MANE Select	NP_000170.1:n.4002-26_4002-25insCTTTTTT
NM_001281492.2:c.3612-26_3612-25insCTTTTTT (MSH6)	NP_001268421.1:n.3612-26_3612-25insCTTTTTT
NM_001281493.2:c.3096-26_3096-25insCTTTTTT (MSH6)	NP_001268422.1:n.3096-26_3096-25insCTTTTTT
NM_001281494.2:c.3096-26_3096-25insCTTTTTT (MSH6)	NP_001268423.1:n.3096-26_3096-25insCTTTTTT