Canonical Allele Identifier: CA2658967464

Gene: MSH6 FBXO11

Linked Data

• gnomAD v4: 2-47806157-TTTTAATTCCTTTGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806158_47806171del , CM000664.2:g.47806158_47806171del	GRCh38
NC_000002.11:g.48033297_48033310del , CM000664.1:g.48033297_48033310del	GRCh37
NC_000002.10:g.47886801_47886814del	NCBI36
NG_007111.1:g.28012_28025del , LRG_219:g.28012_28025del
NG_008397.1:g.104505_104518del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3350-46_3350-33del (MSH6)	ENSP00000406248.2:n.3350-46_3350-33del
ENST00000420813.6:c.3350-46_3350-33del (MSH6)	ENSP00000390382.2:n.3350-46_3350-33del
ENST00000455383.6:c.3350-46_3350-33del (MSH6)	ENSP00000397484.2:n.3350-46_3350-33del
ENST00000700004.2:c.3263-46_3263-33del (MSH6)	ENSP00000514752.2:n.3263-46_3263-33del
ENST00000699999.1:n.4321-46_4321-33del (MSH6)
ENST00000700000.1:c.2081-46_2081-33del (MSH6)	ENSP00000514749.1:n.2081-46_2081-33del
ENST00000700002.1:c.3653-46_3653-33del (MSH6)	ENSP00000514750.1:n.3653-46_3653-33del
ENST00000700003.1:c.1102-46_1102-33del (MSH6)	ENSP00000514751.1:n.1102-46_1102-33del
ENST00000700004.1:c.2420-46_2420-33del (MSH6)	ENSP00000514752.1:n.2420-46_2420-33del
ENST00000700005.1:n.2498-46_2498-33del (MSH6)
ENST00000700006.1:n.4759_4772del (MSH6)
ENST00000700007.1:n.2242-46_2242-33del (MSH6)
ENST00000700008.1:n.1816-46_1816-33del (MSH6)
ENST00000700009.1:n.2265_2278del (MSH6)
ENST00000700010.1:n.1056-46_1056-33del (MSH6)
ENST00000700011.1:n.2941-46_2941-33del (MSH6)
ENST00000682451.1:n.4577_4590del (FBXO11)
ENST00000684712.1:n.4839_4852del (FBXO11)
ENST00000234420.11:c.3647-46_3647-33del (MSH6) MANE Select	ENSP00000234420.5:n.3647-46_3647-33del
ENST00000540021.6:c.3257-46_3257-33del (MSH6)	ENSP00000446475.1:n.3257-46_3257-33del
ENST00000652107.1:c.3350-46_3350-33del (MSH6)	ENSP00000498629.1:n.3350-46_3350-33del
ENST00000673637.1:c.3350-46_3350-33del (MSH6)	ENSP00000501310.1:n.3350-46_3350-33del
ENST00000234420.9:c.3647-46_3647-33del (MSH6)	ENSP00000234420.4:n.3647-46_3647-33del
ENST00000405808.5:c.169+2024_169+2037del (FBXO11)	ENSP00000385127.1:n.169+2024_169+2037del
ENST00000434234.5:c.*124+1823_*124+1836del (FBXO11)	ENSP00000402692.1:n.*124+1823_*124+1836del
ENST00000445503.5:c.*2994-46_*2994-33del (MSH6)	ENSP00000405294.1:n.*2994-46_*2994-33del
ENST00000538136.1:c.2741-46_2741-33del (MSH6)	ENSP00000438580.1:n.2741-46_2741-33del
ENST00000540021.5:c.3257-46_3257-33del (MSH6)	ENSP00000446475.1:n.3257-46_3257-33del
ENST00000614496.4:c.2741-46_2741-33del (MSH6)	ENSP00000477844.1:n.2741-46_2741-33del
ENST00000622629.4:c.551-46_551-33del (MSH6)	ENSP00000482078.1:n.551-46_551-33del
NM_000179.2:c.3647-46_3647-33del , LRG_219t1:c.3647-46_3647-33del (MSH6)	NP_000170.1:n.3647-46_3647-33del
NM_001281492.1:c.3257-46_3257-33del (MSH6)	NP_001268421.1:n.3257-46_3257-33del
NM_001281493.1:c.2741-46_2741-33del (MSH6)	NP_001268422.1:n.2741-46_2741-33del
NM_001281494.1:c.2741-46_2741-33del (MSH6)	NP_001268423.1:n.2741-46_2741-33del
XM_005264271.1:c.3350-46_3350-33del (MSH6)	XP_005264328.1:n.3350-46_3350-33del
XM_011532798.1:c.3464-46_3464-33del (MSH6)	XP_011531100.1:n.3464-46_3464-33del
XM_011532799.1:c.3350-46_3350-33del (MSH6)	XP_011531101.1:n.3350-46_3350-33del
XM_011532800.1:c.3350-46_3350-33del (MSH6)	XP_011531102.1:n.3350-46_3350-33del
XM_024452819.1:c.3647-46_3647-33del (MSH6)	XP_024308587.1:n.3647-46_3647-33del
XM_024452820.1:c.3464-46_3464-33del (MSH6)	XP_024308588.1:n.3464-46_3464-33del
XM_024452821.1:c.3350-46_3350-33del (MSH6)	XP_024308589.1:n.3350-46_3350-33del
XM_024452822.1:c.2741-46_2741-33del (MSH6)	XP_024308590.1:n.2741-46_2741-33del
NM_000179.3:c.3647-46_3647-33del (MSH6) MANE Select	NP_000170.1:n.3647-46_3647-33del
NM_001281492.2:c.3257-46_3257-33del (MSH6)	NP_001268421.1:n.3257-46_3257-33del
NM_001281493.2:c.2741-46_2741-33del (MSH6)	NP_001268422.1:n.2741-46_2741-33del
NM_001281494.2:c.2741-46_2741-33del (MSH6)	NP_001268423.1:n.2741-46_2741-33del