Canonical Allele Identifier: CA46717505

Gene: MSH6 FBXO11

Linked Data

• dbSNP Id: rs960855943
• MyVariant Identifiers: chr2:g.48032880_48032884del (hg19) ; chr2:g.47805741_47805745del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47805743_47805747del , CM000664.2:g.47805743_47805747del	GRCh38
NC_000002.11:g.48032882_48032886del , CM000664.1:g.48032882_48032886del	GRCh37
NC_000002.10:g.47886386_47886390del	NCBI36
NG_007111.1:g.27597_27601del , LRG_219:g.27597_27601del
NG_008397.1:g.104931_104935del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3349+36_3349+40del (MSH6)	ENSP00000406248.2:n.3349+36_3349+40del
ENST00000420813.6:c.3349+36_3349+40del (MSH6)	ENSP00000390382.2:n.3349+36_3349+40del
ENST00000455383.6:c.3349+36_3349+40del (MSH6)	ENSP00000397484.2:n.3349+36_3349+40del
ENST00000700004.2:c.3262+36_3262+40del (MSH6)	ENSP00000514752.2:n.3262+36_3262+40del
ENST00000699999.1:n.4320+36_4320+40del (MSH6)
ENST00000700000.1:c.2080+36_2080+40del (MSH6)	ENSP00000514749.1:n.2080+36_2080+40del
ENST00000700002.1:c.3652+36_3652+40del (MSH6)	ENSP00000514750.1:n.3652+36_3652+40del
ENST00000700003.1:c.1101+36_1101+40del (MSH6)	ENSP00000514751.1:n.1101+36_1101+40del
ENST00000700004.1:c.2419+36_2419+40del (MSH6)	ENSP00000514752.1:n.2419+36_2419+40del
ENST00000700005.1:n.2497+36_2497+40del (MSH6)
ENST00000700006.1:n.4344_4348del (MSH6)
ENST00000700007.1:n.2241+36_2241+40del (MSH6)
ENST00000700008.1:n.1815+36_1815+40del (MSH6)
ENST00000700009.1:n.1850_1854del (MSH6)
ENST00000700010.1:n.1055+36_1055+40del (MSH6)
ENST00000700011.1:n.2940+36_2940+40del (MSH6)
ENST00000234420.11:c.3646+36_3646+40del (MSH6) MANE Select	ENSP00000234420.5:n.3646+36_3646+40del
ENST00000540021.6:c.3256+36_3256+40del (MSH6)	ENSP00000446475.1:n.3256+36_3256+40del
ENST00000652107.1:c.3349+36_3349+40del (MSH6)	ENSP00000498629.1:n.3349+36_3349+40del
ENST00000673637.1:c.3349+36_3349+40del (MSH6)	ENSP00000501310.1:n.3349+36_3349+40del
ENST00000234420.9:c.3646+36_3646+40del (MSH6)	ENSP00000234420.4:n.3646+36_3646+40del
ENST00000405808.5:c.169+2450_169+2454del (FBXO11)	ENSP00000385127.1:n.169+2450_169+2454del
ENST00000434234.5:c.*124+2249_*124+2253del (FBXO11)	ENSP00000402692.1:n.*124+2249_*124+2253del
ENST00000445503.5:c.*2993+36_*2993+40del (MSH6)	ENSP00000405294.1:n.*2993+36_*2993+40del
ENST00000538136.1:c.2740+36_2740+40del (MSH6)	ENSP00000438580.1:n.2740+36_2740+40del
ENST00000540021.5:c.3256+36_3256+40del (MSH6)	ENSP00000446475.1:n.3256+36_3256+40del
ENST00000614496.4:c.2740+36_2740+40del (MSH6)	ENSP00000477844.1:n.2740+36_2740+40del
ENST00000622629.4:c.550+36_550+40del (MSH6)	ENSP00000482078.1:n.550+36_550+40del
NM_000179.2:c.3646+36_3646+40del , LRG_219t1:c.3646+36_3646+40del (MSH6)	NP_000170.1:n.3646+36_3646+40del
NM_001281492.1:c.3256+36_3256+40del (MSH6)	NP_001268421.1:n.3256+36_3256+40del
NM_001281493.1:c.2740+36_2740+40del (MSH6)	NP_001268422.1:n.2740+36_2740+40del
NM_001281494.1:c.2740+36_2740+40del (MSH6)	NP_001268423.1:n.2740+36_2740+40del
XM_005264271.1:c.3349+36_3349+40del (MSH6)	XP_005264328.1:n.3349+36_3349+40del
XM_011532798.1:c.3463+36_3463+40del (MSH6)	XP_011531100.1:n.3463+36_3463+40del
XM_011532799.1:c.3349+36_3349+40del (MSH6)	XP_011531101.1:n.3349+36_3349+40del
XM_011532800.1:c.3349+36_3349+40del (MSH6)	XP_011531102.1:n.3349+36_3349+40del
XM_024452819.1:c.3646+36_3646+40del (MSH6)	XP_024308587.1:n.3646+36_3646+40del
XM_024452820.1:c.3463+36_3463+40del (MSH6)	XP_024308588.1:n.3463+36_3463+40del
XM_024452821.1:c.3349+36_3349+40del (MSH6)	XP_024308589.1:n.3349+36_3349+40del
XM_024452822.1:c.2740+36_2740+40del (MSH6)	XP_024308590.1:n.2740+36_2740+40del
NM_000179.3:c.3646+36_3646+40del (MSH6) MANE Select	NP_000170.1:n.3646+36_3646+40del
NM_001281492.2:c.3256+36_3256+40del (MSH6)	NP_001268421.1:n.3256+36_3256+40del
NM_001281493.2:c.2740+36_2740+40del (MSH6)	NP_001268422.1:n.2740+36_2740+40del
NM_001281494.2:c.2740+36_2740+40del (MSH6)	NP_001268423.1:n.2740+36_2740+40del