Canonical Allele Identifier: CA2496048109

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47798724_47798725delinsAC , CM000664.2:g.47798724_47798725delinsAC	GRCh38
NC_000002.11:g.48025863_48025864delinsAC , CM000664.1:g.48025863_48025864delinsAC	GRCh37
NC_000002.10:g.47879367_47879368delinsAC	NCBI36
NG_007111.1:g.20578_20579delinsAC , LRG_219:g.20578_20579delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.444_445delinsAC (MSH6)	ENSP00000406248.2:p.Lys148=
ENST00000420813.6:c.444_445delinsAC (MSH6)	ENSP00000390382.2:p.Lys148=
ENST00000455383.6:c.444_445delinsAC (MSH6)	ENSP00000397484.2:p.Lys148=
ENST00000700004.2:c.741_742delinsAC (MSH6)	ENSP00000514752.2:p.Lys247=
ENST00000699999.1:n.825_826delinsAC (MSH6)
ENST00000700000.1:c.741_742delinsAC (MSH6)	ENSP00000514749.1:p.Lys247=
ENST00000700002.1:c.747_748delinsAC (MSH6)	ENSP00000514750.1:p.Lys249=
ENST00000700003.1:c.627+2661_627+2662delinsAC (MSH6)	ENSP00000514751.1:n.627+2661_627+2662delinsAC
ENST00000234420.11:c.741_742delinsAC (MSH6) MANE Select	ENSP00000234420.5:p.Lys247=
ENST00000540021.6:c.351_352delinsAC (MSH6)	ENSP00000446475.1:p.Lys117=
ENST00000652107.1:c.444_445delinsAC (MSH6)	ENSP00000498629.1:p.Lys148=
ENST00000673637.1:c.444_445delinsAC (MSH6)	ENSP00000501310.1:p.Lys148=
ENST00000673922.1:n.463_464delinsAC (MSH6)
ENST00000234420.9:c.741_742delinsAC (MSH6)	ENSP00000234420.4:p.Lys247=
ENST00000405808.5:c.170-9285_170-9284delinsGT (FBXO11)	ENSP00000385127.1:n.170-9285_170-9284delinsGT
ENST00000411819.1:c.444_445delinsAC (MSH6)	ENSP00000406248.1:p.Lys148=
ENST00000434234.5:c.*124+9269_*124+9270delinsGT (FBXO11)	ENSP00000402692.1:n.*124+9269_*124+9270delinsGT
ENST00000445503.5:c.*88_*89delinsAC (MSH6)	ENSP00000405294.1:n.*88_*89delinsAC
ENST00000456246.1:c.*229_*230delinsAC (MSH6)	ENSP00000410570.1:n.*229_*230delinsAC
ENST00000538136.1:c.-166_-165delinsAC (MSH6)	ENSP00000438580.1:n.-166_-165delinsAC
ENST00000540021.5:c.351_352delinsAC (MSH6)	ENSP00000446475.1:p.Lys117=
ENST00000614496.4:c.-166_-165delinsAC (MSH6)	ENSP00000477844.1:n.-166_-165delinsAC
ENST00000616033.4:c.738_739delinsAC (MSH6)	ENSP00000480261.1:p.Lys246=
ENST00000622629.4:c.-2356_-2355delinsAC (MSH6)	ENSP00000482078.1:n.-2356_-2355delinsAC
NM_000179.2:c.741_742delinsAC , LRG_219t1:c.741_742delinsAC (MSH6)	NP_000170.1:p.Lys247=
NM_001281492.1:c.351_352delinsAC (MSH6)	NP_001268421.1:p.Lys117=
NM_001281493.1:c.-166_-165delinsAC (MSH6)	NP_001268422.1:n.-166_-165delinsAC
NM_001281494.1:c.-166_-165delinsAC (MSH6)	NP_001268423.1:n.-166_-165delinsAC
XM_005264271.1:c.444_445delinsAC (MSH6)	XP_005264328.1:p.Lys148=
XM_011532798.1:c.558_559delinsAC (MSH6)	XP_011531100.1:p.Lys186=
XM_011532799.1:c.444_445delinsAC (MSH6)	XP_011531101.1:p.Lys148=
XM_011532800.1:c.444_445delinsAC (MSH6)	XP_011531102.1:p.Lys148=
XM_024452819.1:c.741_742delinsAC (MSH6)	XP_024308587.1:p.Lys247=
XM_024452820.1:c.558_559delinsAC (MSH6)	XP_024308588.1:p.Lys186=
XM_024452821.1:c.444_445delinsAC (MSH6)	XP_024308589.1:p.Lys148=
XM_024452822.1:c.-166_-165delinsAC (MSH6)	XP_024308590.1:n.-166_-165delinsAC
NM_000179.3:c.741_742delinsAC (MSH6) MANE Select	NP_000170.1:p.Lys247=
NM_001281492.2:c.351_352delinsAC (MSH6)	NP_001268421.1:p.Lys117=
NM_001281493.2:c.-166_-165delinsAC (MSH6)	NP_001268422.1:n.-166_-165delinsAC
NM_001281494.2:c.-166_-165delinsAC (MSH6)	NP_001268423.1:n.-166_-165delinsAC