Canonical Allele Identifier: CA2658970702

Gene: MSH6 FBXO11

Linked Data

• gnomAD v4: 2-47806931-T-TTC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806931_47806932insTC , CM000664.2:g.47806931_47806932insTC	GRCh38
NC_000002.11:g.48034070_48034071insTC , CM000664.1:g.48034070_48034071insTC	GRCh37
NC_000002.10:g.47887574_47887575insTC	NCBI36
NG_007111.1:g.28785_28786insTC , LRG_219:g.28785_28786insTC
NG_008397.1:g.103744_103745insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.*71_*72insTC (MSH6)	ENSP00000406248.2:n.*71_*72insTC
ENST00000420813.6:c.*71_*72insTC (MSH6)	ENSP00000390382.2:n.*71_*72insTC
ENST00000455383.6:c.*71_*72insTC (MSH6)	ENSP00000397484.2:n.*71_*72insTC
ENST00000700002.1:c.*71_*72insTC (MSH6)	ENSP00000514750.1:n.*71_*72insTC
ENST00000700007.1:n.2749_2750insTC (MSH6)
ENST00000682451.1:n.3816_3817insGA (FBXO11)
ENST00000684712.1:n.4078_4079insGA (FBXO11)
ENST00000234420.11:c.*71_*72insTC (MSH6) MANE Select	ENSP00000234420.5:n.*71_*72insTC
ENST00000403359.8:c.*1186_*1187insGA (FBXO11) MANE Select	ENSP00000384823.4:n.*1186_*1187insGA
ENST00000540021.6:c.*71_*72insTC (MSH6)	ENSP00000446475.1:n.*71_*72insTC
ENST00000652107.1:c.*71_*72insTC (MSH6)	ENSP00000498629.1:n.*71_*72insTC
ENST00000234420.9:c.*71_*72insTC (MSH6)	ENSP00000234420.4:n.*71_*72insTC
ENST00000402508.5:c.*1186_*1187insGA (FBXO11)	ENSP00000385398.1:n.*1186_*1187insGA
ENST00000403359.7:c.*1186_*1187insGA (FBXO11)	ENSP00000384823.3:n.*1186_*1187insGA
ENST00000405808.5:c.169+1263_169+1264insGA (FBXO11)	ENSP00000385127.1:n.169+1263_169+1264insGA
ENST00000434234.5:c.*124+1062_*124+1063insGA (FBXO11)	ENSP00000402692.1:n.*124+1062_*124+1063insGA
ENST00000445503.5:c.*3501_*3502insTC (MSH6)	ENSP00000405294.1:n.*3501_*3502insTC
ENST00000465204.5:n.2978_2979insGA (FBXO11)
ENST00000538136.1:c.*71_*72insTC (MSH6)	ENSP00000438580.1:n.*71_*72insTC
ENST00000540021.5:c.*71_*72insTC (MSH6)	ENSP00000446475.1:n.*71_*72insTC
ENST00000614496.4:c.*71_*72insTC (MSH6)	ENSP00000477844.1:n.*71_*72insTC
ENST00000622629.4:c.*71_*72insTC (MSH6)	ENSP00000482078.1:n.*71_*72insTC
NM_000179.2:c.*71_*72insTC , LRG_219t1:c.*71_*72insTC (MSH6)	NP_000170.1:n.*71_*72insTC
NM_001190274.1:c.*1186_*1187insGA (FBXO11)	NP_001177203.1:n.*1186_*1187insGA
NM_001281492.1:c.*71_*72insTC (MSH6)	NP_001268421.1:n.*71_*72insTC
NM_001281493.1:c.*71_*72insTC (MSH6)	NP_001268422.1:n.*71_*72insTC
NM_001281494.1:c.*71_*72insTC (MSH6)	NP_001268423.1:n.*71_*72insTC
NM_025133.4:c.*1186_*1187insGA (FBXO11)	NP_079409.3:n.*1186_*1187insGA
XM_005264271.1:c.*71_*72insTC (MSH6)	XP_005264328.1:n.*71_*72insTC
XM_005264572.3:c.*1186_*1187insGA (FBXO11)	XP_005264629.1:n.*1186_*1187insGA
XM_005264573.3:c.*1186_*1187insGA (FBXO11)	XP_005264630.1:n.*1186_*1187insGA
XM_011532798.1:c.*71_*72insTC (MSH6)	XP_011531100.1:n.*71_*72insTC
XM_011532799.1:c.*71_*72insTC (MSH6)	XP_011531101.1:n.*71_*72insTC
XM_011532800.1:c.*71_*72insTC (MSH6)	XP_011531102.1:n.*71_*72insTC
XM_005264572.5:c.*1186_*1187insGA (FBXO11)	XP_005264629.1:n.*1186_*1187insGA
XM_005264573.5:c.*1186_*1187insGA (FBXO11)	XP_005264630.1:n.*1186_*1187insGA
XM_017005015.1:c.*1186_*1187insGA (FBXO11)	XP_016860504.1:n.*1186_*1187insGA
XM_017005016.2:c.*1186_*1187insGA (FBXO11)	XP_016860505.1:n.*1186_*1187insGA
XM_017005017.1:c.*1186_*1187insGA (FBXO11)	XP_016860506.1:n.*1186_*1187insGA
XM_024452819.1:c.*71_*72insTC (MSH6)	XP_024308587.1:n.*71_*72insTC
XM_024452820.1:c.*71_*72insTC (MSH6)	XP_024308588.1:n.*71_*72insTC
XM_024452821.1:c.*71_*72insTC (MSH6)	XP_024308589.1:n.*71_*72insTC
XM_024452822.1:c.*71_*72insTC (MSH6)	XP_024308590.1:n.*71_*72insTC
NM_000179.3:c.*71_*72insTC (MSH6) MANE Select	NP_000170.1:n.*71_*72insTC
NM_001190274.2:c.*1186_*1187insGA (FBXO11) MANE Select	NP_001177203.1:n.*1186_*1187insGA
NM_001374325.1:c.*1186_*1187insGA (FBXO11)	NP_001361254.1:n.*1186_*1187insGA
NM_001281492.2:c.*71_*72insTC (MSH6)	NP_001268421.1:n.*71_*72insTC
NM_001281493.2:c.*71_*72insTC (MSH6)	NP_001268422.1:n.*71_*72insTC
NM_001281494.2:c.*71_*72insTC (MSH6)	NP_001268423.1:n.*71_*72insTC