Canonical Allele Identifier: CA1030295081

Gene: MSH6 FBXO11

Linked Data

• dbSNP Id: rs1669982553
• gnomAD v3: 2-47805740-CTA-C
• gnomAD v4: 2-47805740-CTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47805742_47805743del , CM000664.2:g.47805742_47805743del	GRCh38
NC_000002.11:g.48032881_48032882del , CM000664.1:g.48032881_48032882del	GRCh37
NC_000002.10:g.47886385_47886386del	NCBI36
NG_007111.1:g.27596_27597del , LRG_219:g.27596_27597del
NG_008397.1:g.104934_104935del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3349+35_3349+36del (MSH6)	ENSP00000406248.2:n.3349+35_3349+36del
ENST00000420813.6:c.3349+35_3349+36del (MSH6)	ENSP00000390382.2:n.3349+35_3349+36del
ENST00000455383.6:c.3349+35_3349+36del (MSH6)	ENSP00000397484.2:n.3349+35_3349+36del
ENST00000700004.2:c.3262+35_3262+36del (MSH6)	ENSP00000514752.2:n.3262+35_3262+36del
ENST00000699999.1:n.4320+35_4320+36del (MSH6)
ENST00000700000.1:c.2080+35_2080+36del (MSH6)	ENSP00000514749.1:n.2080+35_2080+36del
ENST00000700002.1:c.3652+35_3652+36del (MSH6)	ENSP00000514750.1:n.3652+35_3652+36del
ENST00000700003.1:c.1101+35_1101+36del (MSH6)	ENSP00000514751.1:n.1101+35_1101+36del
ENST00000700004.1:c.2419+35_2419+36del (MSH6)	ENSP00000514752.1:n.2419+35_2419+36del
ENST00000700005.1:n.2497+35_2497+36del (MSH6)
ENST00000700006.1:n.4343_4344del (MSH6)
ENST00000700007.1:n.2241+35_2241+36del (MSH6)
ENST00000700008.1:n.1815+35_1815+36del (MSH6)
ENST00000700009.1:n.1849_1850del (MSH6)
ENST00000700010.1:n.1055+35_1055+36del (MSH6)
ENST00000700011.1:n.2940+35_2940+36del (MSH6)
ENST00000234420.11:c.3646+35_3646+36del (MSH6) MANE Select	ENSP00000234420.5:n.3646+35_3646+36del
ENST00000540021.6:c.3256+35_3256+36del (MSH6)	ENSP00000446475.1:n.3256+35_3256+36del
ENST00000652107.1:c.3349+35_3349+36del (MSH6)	ENSP00000498629.1:n.3349+35_3349+36del
ENST00000673637.1:c.3349+35_3349+36del (MSH6)	ENSP00000501310.1:n.3349+35_3349+36del
ENST00000234420.9:c.3646+35_3646+36del (MSH6)	ENSP00000234420.4:n.3646+35_3646+36del
ENST00000405808.5:c.169+2453_169+2454del (FBXO11)	ENSP00000385127.1:n.169+2453_169+2454del
ENST00000434234.5:c.*124+2252_*124+2253del (FBXO11)	ENSP00000402692.1:n.*124+2252_*124+2253del
ENST00000445503.5:c.*2993+35_*2993+36del (MSH6)	ENSP00000405294.1:n.*2993+35_*2993+36del
ENST00000538136.1:c.2740+35_2740+36del (MSH6)	ENSP00000438580.1:n.2740+35_2740+36del
ENST00000540021.5:c.3256+35_3256+36del (MSH6)	ENSP00000446475.1:n.3256+35_3256+36del
ENST00000614496.4:c.2740+35_2740+36del (MSH6)	ENSP00000477844.1:n.2740+35_2740+36del
ENST00000622629.4:c.550+35_550+36del (MSH6)	ENSP00000482078.1:n.550+35_550+36del
NM_000179.2:c.3646+35_3646+36del , LRG_219t1:c.3646+35_3646+36del (MSH6)	NP_000170.1:n.3646+35_3646+36del
NM_001281492.1:c.3256+35_3256+36del (MSH6)	NP_001268421.1:n.3256+35_3256+36del
NM_001281493.1:c.2740+35_2740+36del (MSH6)	NP_001268422.1:n.2740+35_2740+36del
NM_001281494.1:c.2740+35_2740+36del (MSH6)	NP_001268423.1:n.2740+35_2740+36del
XM_005264271.1:c.3349+35_3349+36del (MSH6)	XP_005264328.1:n.3349+35_3349+36del
XM_011532798.1:c.3463+35_3463+36del (MSH6)	XP_011531100.1:n.3463+35_3463+36del
XM_011532799.1:c.3349+35_3349+36del (MSH6)	XP_011531101.1:n.3349+35_3349+36del
XM_011532800.1:c.3349+35_3349+36del (MSH6)	XP_011531102.1:n.3349+35_3349+36del
XM_024452819.1:c.3646+35_3646+36del (MSH6)	XP_024308587.1:n.3646+35_3646+36del
XM_024452820.1:c.3463+35_3463+36del (MSH6)	XP_024308588.1:n.3463+35_3463+36del
XM_024452821.1:c.3349+35_3349+36del (MSH6)	XP_024308589.1:n.3349+35_3349+36del
XM_024452822.1:c.2740+35_2740+36del (MSH6)	XP_024308590.1:n.2740+35_2740+36del
NM_000179.3:c.3646+35_3646+36del (MSH6) MANE Select	NP_000170.1:n.3646+35_3646+36del
NM_001281492.2:c.3256+35_3256+36del (MSH6)	NP_001268421.1:n.3256+35_3256+36del
NM_001281493.2:c.2740+35_2740+36del (MSH6)	NP_001268422.1:n.2740+35_2740+36del
NM_001281494.2:c.2740+35_2740+36del (MSH6)	NP_001268423.1:n.2740+35_2740+36del