Canonical Allele Identifier: CA2838032270

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47798919_47798928del , CM000664.2:g.47798919_47798928del	GRCh38
NC_000002.11:g.48026058_48026067del , CM000664.1:g.48026058_48026067del	GRCh37
NC_000002.10:g.47879562_47879571del	NCBI36
NG_007111.1:g.20773_20782del , LRG_219:g.20773_20782del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.639_648del (MSH6)	ENSP00000406248.2:p.Lys214GlyfsTer22
ENST00000420813.6:c.639_648del (MSH6)	ENSP00000390382.2:p.Lys214GlyfsTer22
ENST00000455383.6:c.639_648del (MSH6)	ENSP00000397484.2:p.Lys214GlyfsTer22
ENST00000700004.2:c.936_945del (MSH6)	ENSP00000514752.2:p.Lys313GlyfsTer22
ENST00000699999.1:n.1020_1029del (MSH6)
ENST00000700000.1:c.936_945del (MSH6)	ENSP00000514749.1:p.Lys313GlyfsTer22
ENST00000700002.1:c.942_951del (MSH6)	ENSP00000514750.1:p.Lys315GlyfsTer22
ENST00000700003.1:c.627+2856_627+2865del (MSH6)	ENSP00000514751.1:n.627+2856_627+2865del
ENST00000700004.1:c.93_102del (MSH6)	ENSP00000514752.1:p.Lys32GlyfsTer22
ENST00000234420.11:c.936_945del (MSH6) MANE Select	ENSP00000234420.5:p.Lys313GlyfsTer22
ENST00000540021.6:c.546_555del (MSH6)	ENSP00000446475.1:p.Lys183GlyfsTer22
ENST00000652107.1:c.639_648del (MSH6)	ENSP00000498629.1:p.Lys214GlyfsTer22
ENST00000673637.1:c.639_648del (MSH6)	ENSP00000501310.1:p.Lys214GlyfsTer22
ENST00000234420.9:c.936_945del (MSH6)	ENSP00000234420.4:p.Lys313GlyfsTer22
ENST00000405808.5:c.169+9267_169+9276del (FBXO11)	ENSP00000385127.1:n.169+9267_169+9276del
ENST00000434234.5:c.*124+9066_*124+9075del (FBXO11)	ENSP00000402692.1:n.*124+9066_*124+9075del
ENST00000445503.5:c.*283_*292del (MSH6)	ENSP00000405294.1:n.*283_*292del
ENST00000538136.1:c.30_39del (MSH6)	ENSP00000438580.1:p.Lys11GlyfsTer22
ENST00000540021.5:c.546_555del (MSH6)	ENSP00000446475.1:p.Lys183GlyfsTer22
ENST00000614496.4:c.30_39del (MSH6)	ENSP00000477844.1:p.Lys11GlyfsTer22
ENST00000616033.4:c.933_942del (MSH6)	ENSP00000480261.1:p.Lys312GlyfsTer22
ENST00000622629.4:c.-2161_-2152del (MSH6)	ENSP00000482078.1:n.-2161_-2152del
NM_000179.2:c.936_945del , LRG_219t1:c.936_945del (MSH6)	NP_000170.1:p.Lys313GlyfsTer22
NM_001281492.1:c.546_555del (MSH6)	NP_001268421.1:p.Lys183GlyfsTer22
NM_001281493.1:c.30_39del (MSH6)	NP_001268422.1:p.Lys11GlyfsTer22
NM_001281494.1:c.30_39del (MSH6)	NP_001268423.1:p.Lys11GlyfsTer22
XM_005264271.1:c.639_648del (MSH6)	XP_005264328.1:p.Lys214GlyfsTer22
XM_011532798.1:c.753_762del (MSH6)	XP_011531100.1:p.Lys252GlyfsTer22
XM_011532799.1:c.639_648del (MSH6)	XP_011531101.1:p.Lys214GlyfsTer22
XM_011532800.1:c.639_648del (MSH6)	XP_011531102.1:p.Lys214GlyfsTer22
XM_024452819.1:c.936_945del (MSH6)	XP_024308587.1:p.Lys313GlyfsTer22
XM_024452820.1:c.753_762del (MSH6)	XP_024308588.1:p.Lys252GlyfsTer22
XM_024452821.1:c.639_648del (MSH6)	XP_024308589.1:p.Lys214GlyfsTer22
XM_024452822.1:c.30_39del (MSH6)	XP_024308590.1:p.Lys11GlyfsTer22
NM_000179.3:c.936_945del (MSH6) MANE Select	NP_000170.1:p.Lys313GlyfsTer22
NM_001281492.2:c.546_555del (MSH6)	NP_001268421.1:p.Lys183GlyfsTer22
NM_001281493.2:c.30_39del (MSH6)	NP_001268422.1:p.Lys11GlyfsTer22
NM_001281494.2:c.30_39del (MSH6)	NP_001268423.1:p.Lys11GlyfsTer22