Canonical Allele Identifier: CA769464211

Gene: MSH6 FBXO11

Linked Data

• dbSNP Id: rs1285932422
• MyVariant Identifiers: chr2:g.48032660_48032661del (hg19) ; chr2:g.47805521_47805522del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47805523_47805524del , CM000664.2:g.47805523_47805524del	GRCh38
NC_000002.11:g.48032662_48032663del , CM000664.1:g.48032662_48032663del	GRCh37
NC_000002.10:g.47886166_47886167del	NCBI36
NG_007111.1:g.27377_27378del , LRG_219:g.27377_27378del
NG_008397.1:g.105154_105155del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3260-95_3260-94del (MSH6)	ENSP00000406248.2:n.3260-95_3260-94del
ENST00000420813.6:c.3260-95_3260-94del (MSH6)	ENSP00000390382.2:n.3260-95_3260-94del
ENST00000455383.6:c.3260-95_3260-94del (MSH6)	ENSP00000397484.2:n.3260-95_3260-94del
ENST00000700004.2:c.3173-95_3173-94del (MSH6)	ENSP00000514752.2:n.3173-95_3173-94del
ENST00000699999.1:n.4136_4137del (MSH6)
ENST00000700000.1:c.1991-95_1991-94del (MSH6)	ENSP00000514749.1:n.1991-95_1991-94del
ENST00000700002.1:c.3563-95_3563-94del (MSH6)	ENSP00000514750.1:n.3563-95_3563-94del
ENST00000700003.1:c.1012-95_1012-94del (MSH6)	ENSP00000514751.1:n.1012-95_1012-94del
ENST00000700004.1:c.2330-95_2330-94del (MSH6)	ENSP00000514752.1:n.2330-95_2330-94del
ENST00000700005.1:n.2408-95_2408-94del (MSH6)
ENST00000700006.1:n.4124_4125del (MSH6)
ENST00000700007.1:n.2057_2058del (MSH6)
ENST00000700008.1:n.1631_1632del (MSH6)
ENST00000700009.1:n.1630_1631del (MSH6)
ENST00000700010.1:n.966-95_966-94del (MSH6)
ENST00000700011.1:n.2756_2757del (MSH6)
ENST00000234420.11:c.3557-95_3557-94del (MSH6) MANE Select	ENSP00000234420.5:n.3557-95_3557-94del
ENST00000540021.6:c.3167-95_3167-94del (MSH6)	ENSP00000446475.1:n.3167-95_3167-94del
ENST00000652107.1:c.3260-95_3260-94del (MSH6)	ENSP00000498629.1:n.3260-95_3260-94del
ENST00000673637.1:c.3260-95_3260-94del (MSH6)	ENSP00000501310.1:n.3260-95_3260-94del
ENST00000234420.9:c.3557-95_3557-94del (MSH6)	ENSP00000234420.4:n.3557-95_3557-94del
ENST00000405808.5:c.169+2673_169+2674del (FBXO11)	ENSP00000385127.1:n.169+2673_169+2674del
ENST00000434234.5:c.*124+2472_*124+2473del (FBXO11)	ENSP00000402692.1:n.*124+2472_*124+2473del
ENST00000445503.5:c.*2904-95_*2904-94del (MSH6)	ENSP00000405294.1:n.*2904-95_*2904-94del
ENST00000538136.1:c.2651-95_2651-94del (MSH6)	ENSP00000438580.1:n.2651-95_2651-94del
ENST00000540021.5:c.3167-95_3167-94del (MSH6)	ENSP00000446475.1:n.3167-95_3167-94del
ENST00000614496.4:c.2651-95_2651-94del (MSH6)	ENSP00000477844.1:n.2651-95_2651-94del
ENST00000622629.4:c.461-95_461-94del (MSH6)	ENSP00000482078.1:n.461-95_461-94del
NM_000179.2:c.3557-95_3557-94del , LRG_219t1:c.3557-95_3557-94del (MSH6)	NP_000170.1:n.3557-95_3557-94del
NM_001281492.1:c.3167-95_3167-94del (MSH6)	NP_001268421.1:n.3167-95_3167-94del
NM_001281493.1:c.2651-95_2651-94del (MSH6)	NP_001268422.1:n.2651-95_2651-94del
NM_001281494.1:c.2651-95_2651-94del (MSH6)	NP_001268423.1:n.2651-95_2651-94del
XM_005264271.1:c.3260-95_3260-94del (MSH6)	XP_005264328.1:n.3260-95_3260-94del
XM_011532798.1:c.3374-95_3374-94del (MSH6)	XP_011531100.1:n.3374-95_3374-94del
XM_011532799.1:c.3260-95_3260-94del (MSH6)	XP_011531101.1:n.3260-95_3260-94del
XM_011532800.1:c.3260-95_3260-94del (MSH6)	XP_011531102.1:n.3260-95_3260-94del
XM_024452819.1:c.3557-95_3557-94del (MSH6)	XP_024308587.1:n.3557-95_3557-94del
XM_024452820.1:c.3374-95_3374-94del (MSH6)	XP_024308588.1:n.3374-95_3374-94del
XM_024452821.1:c.3260-95_3260-94del (MSH6)	XP_024308589.1:n.3260-95_3260-94del
XM_024452822.1:c.2651-95_2651-94del (MSH6)	XP_024308590.1:n.2651-95_2651-94del
NM_000179.3:c.3557-95_3557-94del (MSH6) MANE Select	NP_000170.1:n.3557-95_3557-94del
NM_001281492.2:c.3167-95_3167-94del (MSH6)	NP_001268421.1:n.3167-95_3167-94del
NM_001281493.2:c.2651-95_2651-94del (MSH6)	NP_001268422.1:n.2651-95_2651-94del
NM_001281494.2:c.2651-95_2651-94del (MSH6)	NP_001268423.1:n.2651-95_2651-94del