Canonical Allele Identifier: CA2496053808

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806039_47806042delinsGGCT , CM000664.2:g.47806039_47806042delinsGGCT	GRCh38
NC_000002.11:g.48033178_48033181delinsGGCT , CM000664.1:g.48033178_48033181delinsGGCT	GRCh37
NC_000002.10:g.47886682_47886685delinsGGCT	NCBI36
NG_007111.1:g.27893_27896delinsGGCT , LRG_219:g.27893_27896delinsGGCT
NG_008397.1:g.104634_104637delinsAGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3350-165_3350-162delinsGGCT (MSH6)	ENSP00000406248.2:n.3350-165_3350-162delinsGGCT
ENST00000420813.6:c.3350-165_3350-162delinsGGCT (MSH6)	ENSP00000390382.2:n.3350-165_3350-162delinsGGCT
ENST00000455383.6:c.3350-165_3350-162delinsGGCT (MSH6)	ENSP00000397484.2:n.3350-165_3350-162delinsGGCT
ENST00000700004.2:c.3263-165_3263-162delinsGGCT (MSH6)	ENSP00000514752.2:n.3263-165_3263-162delinsGGCT
ENST00000699999.1:n.4321-165_4321-162delinsGGCT (MSH6)
ENST00000700000.1:c.2081-165_2081-162delinsGGCT (MSH6)	ENSP00000514749.1:n.2081-165_2081-162delinsGGCT
ENST00000700002.1:c.3653-165_3653-162delinsGGCT (MSH6)	ENSP00000514750.1:n.3653-165_3653-162delinsGGCT
ENST00000700003.1:c.1102-165_1102-162delinsGGCT (MSH6)	ENSP00000514751.1:n.1102-165_1102-162delinsGGCT
ENST00000700004.1:c.2420-165_2420-162delinsGGCT (MSH6)	ENSP00000514752.1:n.2420-165_2420-162delinsGGCT
ENST00000700005.1:n.2498-165_2498-162delinsGGCT (MSH6)
ENST00000700006.1:n.4640_4643delinsGGCT (MSH6)
ENST00000700007.1:n.2242-165_2242-162delinsGGCT (MSH6)
ENST00000700008.1:n.1816-165_1816-162delinsGGCT (MSH6)
ENST00000700009.1:n.2146_2149delinsGGCT (MSH6)
ENST00000700010.1:n.1056-165_1056-162delinsGGCT (MSH6)
ENST00000700011.1:n.2941-165_2941-162delinsGGCT (MSH6)
ENST00000234420.11:c.3647-165_3647-162delinsGGCT (MSH6) MANE Select	ENSP00000234420.5:n.3647-165_3647-162delinsGGCT
ENST00000540021.6:c.3257-165_3257-162delinsGGCT (MSH6)	ENSP00000446475.1:n.3257-165_3257-162delinsGGCT
ENST00000652107.1:c.3350-165_3350-162delinsGGCT (MSH6)	ENSP00000498629.1:n.3350-165_3350-162delinsGGCT
ENST00000673637.1:c.3350-165_3350-162delinsGGCT (MSH6)	ENSP00000501310.1:n.3350-165_3350-162delinsGGCT
ENST00000234420.9:c.3647-165_3647-162delinsGGCT (MSH6)	ENSP00000234420.4:n.3647-165_3647-162delinsGGCT
ENST00000405808.5:c.169+2153_169+2156delinsAGCC (FBXO11)	ENSP00000385127.1:n.169+2153_169+2156delinsAGCC
ENST00000434234.5:c.*124+1952_*124+1955delinsAGCC (FBXO11)	ENSP00000402692.1:n.*124+1952_*124+1955delinsAGCC
ENST00000445503.5:c.*2994-165_*2994-162delinsGGCT (MSH6)	ENSP00000405294.1:n.*2994-165_*2994-162delinsGGCT
ENST00000538136.1:c.2741-165_2741-162delinsGGCT (MSH6)	ENSP00000438580.1:n.2741-165_2741-162delinsGGCT
ENST00000540021.5:c.3257-165_3257-162delinsGGCT (MSH6)	ENSP00000446475.1:n.3257-165_3257-162delinsGGCT
ENST00000614496.4:c.2741-165_2741-162delinsGGCT (MSH6)	ENSP00000477844.1:n.2741-165_2741-162delinsGGCT
ENST00000622629.4:c.551-165_551-162delinsGGCT (MSH6)	ENSP00000482078.1:n.551-165_551-162delinsGGCT
NM_000179.2:c.3647-165_3647-162delinsGGCT , LRG_219t1:c.3647-165_3647-162delinsGGCT (MSH6)	NP_000170.1:n.3647-165_3647-162delinsGGCT
NM_001281492.1:c.3257-165_3257-162delinsGGCT (MSH6)	NP_001268421.1:n.3257-165_3257-162delinsGGCT
NM_001281493.1:c.2741-165_2741-162delinsGGCT (MSH6)	NP_001268422.1:n.2741-165_2741-162delinsGGCT
NM_001281494.1:c.2741-165_2741-162delinsGGCT (MSH6)	NP_001268423.1:n.2741-165_2741-162delinsGGCT
XM_005264271.1:c.3350-165_3350-162delinsGGCT (MSH6)	XP_005264328.1:n.3350-165_3350-162delinsGGCT
XM_011532798.1:c.3464-165_3464-162delinsGGCT (MSH6)	XP_011531100.1:n.3464-165_3464-162delinsGGCT
XM_011532799.1:c.3350-165_3350-162delinsGGCT (MSH6)	XP_011531101.1:n.3350-165_3350-162delinsGGCT
XM_011532800.1:c.3350-165_3350-162delinsGGCT (MSH6)	XP_011531102.1:n.3350-165_3350-162delinsGGCT
XM_024452819.1:c.3647-165_3647-162delinsGGCT (MSH6)	XP_024308587.1:n.3647-165_3647-162delinsGGCT
XM_024452820.1:c.3464-165_3464-162delinsGGCT (MSH6)	XP_024308588.1:n.3464-165_3464-162delinsGGCT
XM_024452821.1:c.3350-165_3350-162delinsGGCT (MSH6)	XP_024308589.1:n.3350-165_3350-162delinsGGCT
XM_024452822.1:c.2741-165_2741-162delinsGGCT (MSH6)	XP_024308590.1:n.2741-165_2741-162delinsGGCT
NM_000179.3:c.3647-165_3647-162delinsGGCT (MSH6) MANE Select	NP_000170.1:n.3647-165_3647-162delinsGGCT
NM_001281492.2:c.3257-165_3257-162delinsGGCT (MSH6)	NP_001268421.1:n.3257-165_3257-162delinsGGCT
NM_001281493.2:c.2741-165_2741-162delinsGGCT (MSH6)	NP_001268422.1:n.2741-165_2741-162delinsGGCT
NM_001281494.2:c.2741-165_2741-162delinsGGCT (MSH6)	NP_001268423.1:n.2741-165_2741-162delinsGGCT