Canonical Allele Identifier: CA2496052962

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47805022_47805025delinsTGTC , CM000664.2:g.47805022_47805025delinsTGTC	GRCh38
NC_000002.11:g.48032161_48032164delinsTGTC , CM000664.1:g.48032161_48032164delinsTGTC	GRCh37
NC_000002.10:g.47885665_47885668delinsTGTC	NCBI36
NG_007111.1:g.26876_26879delinsTGTC , LRG_219:g.26876_26879delinsTGTC
NG_008397.1:g.105651_105654delinsGACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3254_3257delinsTGTC (MSH6)	ENSP00000406248.2:p.Met1085=
ENST00000420813.6:c.3254_3257delinsTGTC (MSH6)	ENSP00000390382.2:p.Met1085=
ENST00000455383.6:c.3254_3257delinsTGTC (MSH6)	ENSP00000397484.2:p.Met1085=
ENST00000700004.2:c.3173-596_3173-593delinsTGTC (MSH6)	ENSP00000514752.2:n.3173-596_3173-593delinsTGTC
ENST00000699999.1:n.3635_3638delinsTGTC (MSH6)
ENST00000700000.1:c.1985_1988delinsTGTC (MSH6)	ENSP00000514749.1:p.Met662=
ENST00000700002.1:c.3557_3560delinsTGTC (MSH6)	ENSP00000514750.1:p.Met1186=
ENST00000700003.1:c.1006_1009delinsTGTC (MSH6)	ENSP00000514751.1:n.1006_1009delinsTGTC
ENST00000700004.1:c.2330-596_2330-593delinsTGTC (MSH6)	ENSP00000514752.1:n.2330-596_2330-593delinsTGTC
ENST00000700005.1:n.2402_2405delinsTGTC (MSH6)
ENST00000700006.1:n.3623_3626delinsTGTC (MSH6)
ENST00000700007.1:n.1556_1559delinsTGTC (MSH6)
ENST00000700008.1:n.1130_1133delinsTGTC (MSH6)
ENST00000700009.1:n.1129_1132delinsTGTC (MSH6)
ENST00000700010.1:n.960_963delinsTGTC (MSH6)
ENST00000700011.1:n.2255_2258delinsTGTC (MSH6)
ENST00000234420.11:c.3551_3554delinsTGTC (MSH6) MANE Select	ENSP00000234420.5:p.Met1184=
ENST00000540021.6:c.3161_3164delinsTGTC (MSH6)	ENSP00000446475.1:p.Met1054=
ENST00000652107.1:c.3254_3257delinsTGTC (MSH6)	ENSP00000498629.1:p.Met1085=
ENST00000673637.1:c.3254_3257delinsTGTC (MSH6)	ENSP00000501310.1:p.Met1085=
ENST00000234420.9:c.3551_3554delinsTGTC (MSH6)	ENSP00000234420.4:p.Met1184=
ENST00000405808.5:c.169+3170_169+3173delinsGACA (FBXO11)	ENSP00000385127.1:n.169+3170_169+3173delinsGACA
ENST00000434234.5:c.*124+2969_*124+2972delinsGACA (FBXO11)	ENSP00000402692.1:n.*124+2969_*124+2972delinsGACA
ENST00000445503.5:c.*2898_*2901delinsTGTC (MSH6)	ENSP00000405294.1:n.*2898_*2901delinsTGTC
ENST00000538136.1:c.2645_2648delinsTGTC (MSH6)	ENSP00000438580.1:p.Met882=
ENST00000540021.5:c.3161_3164delinsTGTC (MSH6)	ENSP00000446475.1:p.Met1054=
ENST00000614496.4:c.2645_2648delinsTGTC (MSH6)	ENSP00000477844.1:p.Met882=
ENST00000622629.4:c.455_458delinsTGTC (MSH6)	ENSP00000482078.1:p.Met152=
NM_000179.2:c.3551_3554delinsTGTC , LRG_219t1:c.3551_3554delinsTGTC (MSH6)	NP_000170.1:p.Met1184=
NM_001281492.1:c.3161_3164delinsTGTC (MSH6)	NP_001268421.1:p.Met1054=
NM_001281493.1:c.2645_2648delinsTGTC (MSH6)	NP_001268422.1:p.Met882=
NM_001281494.1:c.2645_2648delinsTGTC (MSH6)	NP_001268423.1:p.Met882=
XM_005264271.1:c.3254_3257delinsTGTC (MSH6)	XP_005264328.1:p.Met1085=
XM_011532798.1:c.3368_3371delinsTGTC (MSH6)	XP_011531100.1:p.Met1123=
XM_011532799.1:c.3254_3257delinsTGTC (MSH6)	XP_011531101.1:p.Met1085=
XM_011532800.1:c.3254_3257delinsTGTC (MSH6)	XP_011531102.1:p.Met1085=
XM_024452819.1:c.3551_3554delinsTGTC (MSH6)	XP_024308587.1:p.Met1184=
XM_024452820.1:c.3368_3371delinsTGTC (MSH6)	XP_024308588.1:p.Met1123=
XM_024452821.1:c.3254_3257delinsTGTC (MSH6)	XP_024308589.1:p.Met1085=
XM_024452822.1:c.2645_2648delinsTGTC (MSH6)	XP_024308590.1:p.Met882=
NM_000179.3:c.3551_3554delinsTGTC (MSH6) MANE Select	NP_000170.1:p.Met1184=
NM_001281492.2:c.3161_3164delinsTGTC (MSH6)	NP_001268421.1:p.Met1054=
NM_001281493.2:c.2645_2648delinsTGTC (MSH6)	NP_001268422.1:p.Met882=
NM_001281494.2:c.2645_2648delinsTGTC (MSH6)	NP_001268423.1:p.Met882=