Canonical Allele Identifier: CA2496048049

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47798657_47798663delinsTTGAGAG , CM000664.2:g.47798657_47798663delinsTTGAGAG	GRCh38
NC_000002.11:g.48025796_48025802delinsTTGAGAG , CM000664.1:g.48025796_48025802delinsTTGAGAG	GRCh37
NC_000002.10:g.47879300_47879306delinsTTGAGAG	NCBI36
NG_007111.1:g.20511_20517delinsTTGAGAG , LRG_219:g.20511_20517delinsTTGAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.377_383delinsTTGAGAG (MSH6)	ENSP00000406248.2:p.Ile126=
ENST00000420813.6:c.377_383delinsTTGAGAG (MSH6)	ENSP00000390382.2:p.Ile126=
ENST00000455383.6:c.377_383delinsTTGAGAG (MSH6)	ENSP00000397484.2:p.Ile126=
ENST00000700004.2:c.674_680delinsTTGAGAG (MSH6)	ENSP00000514752.2:p.Ile225=
ENST00000699999.1:n.758_764delinsTTGAGAG (MSH6)
ENST00000700000.1:c.674_680delinsTTGAGAG (MSH6)	ENSP00000514749.1:p.Ile225=
ENST00000700002.1:c.680_686delinsTTGAGAG (MSH6)	ENSP00000514750.1:p.Ile227=
ENST00000700003.1:c.627+2594_627+2600delinsTTGAGAG (MSH6)	ENSP00000514751.1:n.627+2594_627+2600delinsTTGAGAG
ENST00000234420.11:c.674_680delinsTTGAGAG (MSH6) MANE Select	ENSP00000234420.5:p.Ile225=
ENST00000540021.6:c.284_290delinsTTGAGAG (MSH6)	ENSP00000446475.1:p.Ile95=
ENST00000652107.1:c.377_383delinsTTGAGAG (MSH6)	ENSP00000498629.1:p.Ile126=
ENST00000673637.1:c.377_383delinsTTGAGAG (MSH6)	ENSP00000501310.1:p.Ile126=
ENST00000673922.1:n.396_402delinsTTGAGAG (MSH6)
ENST00000234420.9:c.674_680delinsTTGAGAG (MSH6)	ENSP00000234420.4:p.Ile225=
ENST00000405808.5:c.170-9223_170-9217delinsCTCTCAA (FBXO11)	ENSP00000385127.1:n.170-9223_170-9217delinsCTCTCAA
ENST00000411819.1:c.377_383delinsTTGAGAG (MSH6)	ENSP00000406248.1:p.Ile126=
ENST00000434234.5:c.*125-9223_*125-9217delinsCTCTCAA (FBXO11)	ENSP00000402692.1:n.*125-9223_*125-9217delinsCTCTCAA
ENST00000445503.5:c.*21_*27delinsTTGAGAG (MSH6)	ENSP00000405294.1:n.*21_*27delinsTTGAGAG
ENST00000456246.1:c.*162_*168delinsTTGAGAG (MSH6)	ENSP00000410570.1:n.*162_*168delinsTTGAGAG
ENST00000538136.1:c.-233_-227delinsTTGAGAG (MSH6)	ENSP00000438580.1:n.-233_-227delinsTTGAGAG
ENST00000540021.5:c.284_290delinsTTGAGAG (MSH6)	ENSP00000446475.1:p.Ile95=
ENST00000614496.4:c.-233_-227delinsTTGAGAG (MSH6)	ENSP00000477844.1:n.-233_-227delinsTTGAGAG
ENST00000616033.4:c.671_677delinsTTGAGAG (MSH6)	ENSP00000480261.1:p.Ile224=
ENST00000622629.4:c.-2423_-2417delinsTTGAGAG (MSH6)	ENSP00000482078.1:n.-2423_-2417delinsTTGAGAG
NM_000179.2:c.674_680delinsTTGAGAG , LRG_219t1:c.674_680delinsTTGAGAG (MSH6)	NP_000170.1:p.Ile225=
NM_001281492.1:c.284_290delinsTTGAGAG (MSH6)	NP_001268421.1:p.Ile95=
NM_001281493.1:c.-233_-227delinsTTGAGAG (MSH6)	NP_001268422.1:n.-233_-227delinsTTGAGAG
NM_001281494.1:c.-233_-227delinsTTGAGAG (MSH6)	NP_001268423.1:n.-233_-227delinsTTGAGAG
XM_005264271.1:c.377_383delinsTTGAGAG (MSH6)	XP_005264328.1:p.Ile126=
XM_011532798.1:c.491_497delinsTTGAGAG (MSH6)	XP_011531100.1:p.Ile164=
XM_011532799.1:c.377_383delinsTTGAGAG (MSH6)	XP_011531101.1:p.Ile126=
XM_011532800.1:c.377_383delinsTTGAGAG (MSH6)	XP_011531102.1:p.Ile126=
XM_024452819.1:c.674_680delinsTTGAGAG (MSH6)	XP_024308587.1:p.Ile225=
XM_024452820.1:c.491_497delinsTTGAGAG (MSH6)	XP_024308588.1:p.Ile164=
XM_024452821.1:c.377_383delinsTTGAGAG (MSH6)	XP_024308589.1:p.Ile126=
XM_024452822.1:c.-233_-227delinsTTGAGAG (MSH6)	XP_024308590.1:n.-233_-227delinsTTGAGAG
NM_000179.3:c.674_680delinsTTGAGAG (MSH6) MANE Select	NP_000170.1:p.Ile225=
NM_001281492.2:c.284_290delinsTTGAGAG (MSH6)	NP_001268421.1:p.Ile95=
NM_001281493.2:c.-233_-227delinsTTGAGAG (MSH6)	NP_001268422.1:n.-233_-227delinsTTGAGAG
NM_001281494.2:c.-233_-227delinsTTGAGAG (MSH6)	NP_001268423.1:n.-233_-227delinsTTGAGAG