Canonical Allele Identifier: CA2658967062

Gene: MSH6 FBXO11

Linked Data

• gnomAD v4: 2-47805709-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47805711del , CM000664.2:g.47805711del	GRCh38
NC_000002.11:g.48032850del , CM000664.1:g.48032850del	GRCh37
NC_000002.10:g.47886354del	NCBI36
NG_007111.1:g.27565del , LRG_219:g.27565del
NG_008397.1:g.104966del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3349+4del (MSH6)	ENSP00000406248.2:n.3349+4del
ENST00000420813.6:c.3349+4del (MSH6)	ENSP00000390382.2:n.3349+4del
ENST00000455383.6:c.3349+4del (MSH6)	ENSP00000397484.2:n.3349+4del
ENST00000700004.2:c.3262+4del (MSH6)	ENSP00000514752.2:n.3262+4del
ENST00000699999.1:n.4320+4del (MSH6)
ENST00000700000.1:c.2080+4del (MSH6)	ENSP00000514749.1:n.2080+4del
ENST00000700002.1:c.3652+4del (MSH6)	ENSP00000514750.1:n.3652+4del
ENST00000700003.1:c.1101+4del (MSH6)	ENSP00000514751.1:n.1101+4del
ENST00000700004.1:c.2419+4del (MSH6)	ENSP00000514752.1:n.2419+4del
ENST00000700005.1:n.2497+4del (MSH6)
ENST00000700006.1:n.4312del (MSH6)
ENST00000700007.1:n.2241+4del (MSH6)
ENST00000700008.1:n.1815+4del (MSH6)
ENST00000700009.1:n.1818del (MSH6)
ENST00000700010.1:n.1055+4del (MSH6)
ENST00000700011.1:n.2940+4del (MSH6)
ENST00000234420.11:c.3646+4del (MSH6) MANE Select	ENSP00000234420.5:n.3646+4del
ENST00000540021.6:c.3256+4del (MSH6)	ENSP00000446475.1:n.3256+4del
ENST00000652107.1:c.3349+4del (MSH6)	ENSP00000498629.1:n.3349+4del
ENST00000673637.1:c.3349+4del (MSH6)	ENSP00000501310.1:n.3349+4del
ENST00000234420.9:c.3646+4del (MSH6)	ENSP00000234420.4:n.3646+4del
ENST00000405808.5:c.169+2485del (FBXO11)	ENSP00000385127.1:n.169+2485del
ENST00000434234.5:c.*124+2284del (FBXO11)	ENSP00000402692.1:n.*124+2284del
ENST00000445503.5:c.*2993+4del (MSH6)	ENSP00000405294.1:n.*2993+4del
ENST00000538136.1:c.2740+4del (MSH6)	ENSP00000438580.1:n.2740+4del
ENST00000540021.5:c.3256+4del (MSH6)	ENSP00000446475.1:n.3256+4del
ENST00000614496.4:c.2740+4del (MSH6)	ENSP00000477844.1:n.2740+4del
ENST00000622629.4:c.550+4del (MSH6)	ENSP00000482078.1:n.550+4del
NM_000179.2:c.3646+4del , LRG_219t1:c.3646+4del (MSH6)	NP_000170.1:n.3646+4del
NM_001281492.1:c.3256+4del (MSH6)	NP_001268421.1:n.3256+4del
NM_001281493.1:c.2740+4del (MSH6)	NP_001268422.1:n.2740+4del
NM_001281494.1:c.2740+4del (MSH6)	NP_001268423.1:n.2740+4del
XM_005264271.1:c.3349+4del (MSH6)	XP_005264328.1:n.3349+4del
XM_011532798.1:c.3463+4del (MSH6)	XP_011531100.1:n.3463+4del
XM_011532799.1:c.3349+4del (MSH6)	XP_011531101.1:n.3349+4del
XM_011532800.1:c.3349+4del (MSH6)	XP_011531102.1:n.3349+4del
XM_024452819.1:c.3646+4del (MSH6)	XP_024308587.1:n.3646+4del
XM_024452820.1:c.3463+4del (MSH6)	XP_024308588.1:n.3463+4del
XM_024452821.1:c.3349+4del (MSH6)	XP_024308589.1:n.3349+4del
XM_024452822.1:c.2740+4del (MSH6)	XP_024308590.1:n.2740+4del
NM_000179.3:c.3646+4del (MSH6) MANE Select	NP_000170.1:n.3646+4del
NM_001281492.2:c.3256+4del (MSH6)	NP_001268421.1:n.3256+4del
NM_001281493.2:c.2740+4del (MSH6)	NP_001268422.1:n.2740+4del
NM_001281494.2:c.2740+4del (MSH6)	NP_001268423.1:n.2740+4del