Canonical Allele Identifier: CA3062864672

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47803672_47803676delinsTGCTA , CM000664.2:g.47803672_47803676delinsTGCTA	GRCh38
NC_000002.11:g.48030811_48030815delinsTGCTA , CM000664.1:g.48030811_48030815delinsTGCTA	GRCh37
NC_000002.10:g.47884315_47884319delinsTGCTA	NCBI36
NG_007111.1:g.25526_25530delinsTGCTA , LRG_219:g.25526_25530delinsTGCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3128_3132delinsTGCTA (MSH6)	ENSP00000406248.2:p.Thr1043Met
ENST00000420813.6:c.3128_3132delinsTGCTA (MSH6)	ENSP00000390382.2:p.Thr1043Met
ENST00000455383.6:c.3128_3132delinsTGCTA (MSH6)	ENSP00000397484.2:p.Thr1043Met
ENST00000700004.2:c.3173-1946_3173-1942delinsTGCTA (MSH6)	ENSP00000514752.2:n.3173-1946_3173-1942delinsTGCTA
ENST00000699999.1:n.3509_3513delinsTGCTA (MSH6)
ENST00000700000.1:c.1859_1863delinsTGCTA (MSH6)	ENSP00000514749.1:p.Thr620Met
ENST00000700002.1:c.3431_3435delinsTGCTA (MSH6)	ENSP00000514750.1:p.Thr1144Met
ENST00000700003.1:c.880_884delinsTGCTA (MSH6)	ENSP00000514751.1:n.880_884delinsTGCTA
ENST00000700004.1:c.2330-1946_2330-1942delinsTGCTA (MSH6)	ENSP00000514752.1:n.2330-1946_2330-1942delinsTGCTA
ENST00000700005.1:n.2276_2280delinsTGCTA (MSH6)
ENST00000700006.1:n.2273_2277delinsTGCTA (MSH6)
ENST00000700007.1:n.1430_1434delinsTGCTA (MSH6)
ENST00000700008.1:n.1004_1008delinsTGCTA (MSH6)
ENST00000700009.1:n.1003_1007delinsTGCTA (MSH6)
ENST00000700010.1:n.834_838delinsTGCTA (MSH6)
ENST00000700011.1:n.905_909delinsTGCTA (MSH6)
ENST00000234420.11:c.3425_3429delinsTGCTA (MSH6) MANE Select	ENSP00000234420.5:p.Thr1142Met
ENST00000540021.6:c.3035_3039delinsTGCTA (MSH6)	ENSP00000446475.1:p.Thr1012Met
ENST00000652107.1:c.3128_3132delinsTGCTA (MSH6)	ENSP00000498629.1:p.Thr1043Met
ENST00000673637.1:c.3128_3132delinsTGCTA (MSH6)	ENSP00000501310.1:p.Thr1043Met
ENST00000234420.9:c.3425_3429delinsTGCTA (MSH6)	ENSP00000234420.4:p.Thr1142Met
ENST00000405808.5:c.169+4519_169+4523delinsTAGCA (FBXO11)	ENSP00000385127.1:n.169+4519_169+4523delinsTAGCA
ENST00000434234.5:c.*124+4318_*124+4322delinsTAGCA (FBXO11)	ENSP00000402692.1:n.*124+4318_*124+4322delinsTAGCA
ENST00000445503.5:c.*2772_*2776delinsTGCTA (MSH6)	ENSP00000405294.1:n.*2772_*2776delinsTGCTA
ENST00000538136.1:c.2519_2523delinsTGCTA (MSH6)	ENSP00000438580.1:p.Thr840Met
ENST00000540021.5:c.3035_3039delinsTGCTA (MSH6)	ENSP00000446475.1:p.Thr1012Met
ENST00000614496.4:c.2519_2523delinsTGCTA (MSH6)	ENSP00000477844.1:p.Thr840Met
ENST00000622629.4:c.328_332delinsTGCTA (MSH6)	ENSP00000482078.1:p.Arg110CysfsTer2
NM_000179.2:c.3425_3429delinsTGCTA , LRG_219t1:c.3425_3429delinsTGCTA (MSH6)	NP_000170.1:p.Thr1142Met
NM_001281492.1:c.3035_3039delinsTGCTA (MSH6)	NP_001268421.1:p.Thr1012Met
NM_001281493.1:c.2519_2523delinsTGCTA (MSH6)	NP_001268422.1:p.Thr840Met
NM_001281494.1:c.2519_2523delinsTGCTA (MSH6)	NP_001268423.1:p.Thr840Met
XM_005264271.1:c.3128_3132delinsTGCTA (MSH6)	XP_005264328.1:p.Thr1043Met
XM_011532798.1:c.3242_3246delinsTGCTA (MSH6)	XP_011531100.1:p.Thr1081Met
XM_011532799.1:c.3128_3132delinsTGCTA (MSH6)	XP_011531101.1:p.Thr1043Met
XM_011532800.1:c.3128_3132delinsTGCTA (MSH6)	XP_011531102.1:p.Thr1043Met
XM_024452819.1:c.3425_3429delinsTGCTA (MSH6)	XP_024308587.1:p.Thr1142Met
XM_024452820.1:c.3242_3246delinsTGCTA (MSH6)	XP_024308588.1:p.Thr1081Met
XM_024452821.1:c.3128_3132delinsTGCTA (MSH6)	XP_024308589.1:p.Thr1043Met
XM_024452822.1:c.2519_2523delinsTGCTA (MSH6)	XP_024308590.1:p.Thr840Met
NM_000179.3:c.3425_3429delinsTGCTA (MSH6) MANE Select	NP_000170.1:p.Thr1142Met
NM_001281492.2:c.3035_3039delinsTGCTA (MSH6)	NP_001268421.1:p.Thr1012Met
NM_001281493.2:c.2519_2523delinsTGCTA (MSH6)	NP_001268422.1:p.Thr840Met
NM_001281494.2:c.2519_2523delinsTGCTA (MSH6)	NP_001268423.1:p.Thr840Met