Canonical Allele Identifier: CA013241

Gene: MSH6 FBXO11

Linked Data

• dbSNP Id: rs587779268
• MyVariant Identifiers: chr2:g.48032127_48032138del (hg19) ; chr2:g.47804988_47804999del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47804988_47804999del , CM000664.2:g.47804988_47804999del	GRCh38
NC_000002.11:g.48032127_48032138del , CM000664.1:g.48032127_48032138del	GRCh37
NC_000002.10:g.47885631_47885642del	NCBI36
NG_007111.1:g.26842_26853del , LRG_219:g.26842_26853del
NG_008397.1:g.105681_105692del

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.3220_3231del (MSH6)	ENSP00000406248.2:p.Val1074_Arg1077del
ENST00000420813.6:c.3220_3231del (MSH6)	ENSP00000390382.2:p.Val1074_Arg1077del
ENST00000455383.6:c.3220_3231del (MSH6)	ENSP00000397484.2:p.Val1074_Arg1077del
ENST00000700004.2:c.3173-630_3173-619del (MSH6)	ENSP00000514752.2:n.3173-630_3173-619del
ENST00000699999.1:n.3601_3612del (MSH6)
ENST00000700000.1:c.1951_1962del (MSH6)	ENSP00000514749.1:p.Val651_Arg654del
ENST00000700002.1:c.3523_3534del (MSH6)	ENSP00000514750.1:p.Val1175_Arg1178del
ENST00000700003.1:c.972_983del (MSH6)	ENSP00000514751.1:n.972_983del
ENST00000700004.1:c.2330-630_2330-619del (MSH6)	ENSP00000514752.1:n.2330-630_2330-619del
ENST00000700005.1:n.2368_2379del (MSH6)
ENST00000700006.1:n.3589_3600del (MSH6)
ENST00000700007.1:n.1522_1533del (MSH6)
ENST00000700008.1:n.1096_1107del (MSH6)
ENST00000700009.1:n.1095_1106del (MSH6)
ENST00000700010.1:n.926_937del (MSH6)
ENST00000700011.1:n.2221_2232del (MSH6)
ENST00000234420.11:c.3517_3528del (MSH6) MANE Select	ENSP00000234420.5:p.Val1173_Arg1176del
ENST00000540021.6:c.3127_3138del (MSH6)	ENSP00000446475.1:p.Val1043_Arg1046del
ENST00000652107.1:c.3220_3231del (MSH6)	ENSP00000498629.1:p.Val1074_Arg1077del
ENST00000673637.1:c.3220_3231del (MSH6)	ENSP00000501310.1:p.Val1074_Arg1077del
ENST00000234420.9:c.3517_3528del (MSH6)	ENSP00000234420.4:p.Val1173_Arg1176del
ENST00000405808.5:c.169+3200_169+3211del (FBXO11)	ENSP00000385127.1:n.169+3200_169+3211del
ENST00000434234.5:c.*124+2999_*124+3010del (FBXO11)	ENSP00000402692.1:n.*124+2999_*124+3010de...
ENST00000445503.5:c.*2864_*2875del (MSH6)	ENSP00000405294.1:n.*2864_*2875del
ENST00000538136.1:c.2611_2622del (MSH6)	ENSP00000438580.1:p.Val871_Arg874del
ENST00000540021.5:c.3127_3138del (MSH6)	ENSP00000446475.1:p.Val1043_Arg1046del
ENST00000614496.4:c.2611_2622del (MSH6)	ENSP00000477844.1:p.Val871_Arg874del
ENST00000622629.4:c.421_432del (MSH6)	ENSP00000482078.1:p.Val141_Arg144del
NM_000179.2:c.3517_3528del , LRG_219t1:c.3517_3528del (MSH6)	NP_000170.1:p.Val1173_Arg1176del
NM_001281492.1:c.3127_3138del (MSH6)	NP_001268421.1:p.Val1043_Arg1046del
NM_001281493.1:c.2611_2622del (MSH6)	NP_001268422.1:p.Val871_Arg874del
NM_001281494.1:c.2611_2622del (MSH6)	NP_001268423.1:p.Val871_Arg874del
XM_005264271.1:c.3220_3231del (MSH6)	XP_005264328.1:p.Val1074_Arg1077del
XM_011532798.1:c.3334_3345del (MSH6)	XP_011531100.1:p.Val1112_Arg1115del
XM_011532799.1:c.3220_3231del (MSH6)	XP_011531101.1:p.Val1074_Arg1077del
XM_011532800.1:c.3220_3231del (MSH6)	XP_011531102.1:p.Val1074_Arg1077del
XM_024452819.1:c.3517_3528del (MSH6)	XP_024308587.1:p.Val1173_Arg1176del
XM_024452820.1:c.3334_3345del (MSH6)	XP_024308588.1:p.Val1112_Arg1115del
XM_024452821.1:c.3220_3231del (MSH6)	XP_024308589.1:p.Val1074_Arg1077del
XM_024452822.1:c.2611_2622del (MSH6)	XP_024308590.1:p.Val871_Arg874del
NM_000179.3:c.3517_3528del (MSH6) MANE Select	NP_000170.1:p.Val1173_Arg1176del
NM_001281492.2:c.3127_3138del (MSH6)	NP_001268421.1:p.Val1043_Arg1046del
NM_001281493.2:c.2611_2622del (MSH6)	NP_001268422.1:p.Val871_Arg874del
NM_001281494.2:c.2611_2622del (MSH6)	NP_001268423.1:p.Val871_Arg874del