Canonical Allele Identifier: CA2496054230

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47806351_47806381delinsGACATATGGTATGTGCAAATTGTTTTTTTCC , CM000664.2:g.47806351_47806381delinsGACATATGGTATGTGCAAATTGTTTTTTTCC GRCh38
NC_000002.11:g.48033490_48033520delinsGACATATGGTATGTGCAAATTGTTTTTTTCC , CM000664.1:g.48033490_48033520delinsGACATATGGTATGTGCAAATTGTTTTTTTCC GRCh37
NC_000002.10:g.47886994_47887024delinsGACATATGGTATGTGCAAATTGTTTTTTTCC NCBI36
NG_007111.1:g.28205_28235delinsGACATATGGTATGTGCAAATTGTTTTTTTCC , LRG_219:g.28205_28235delinsGACATATGGTATGTGCAAATTGTTTTTTTCC
NG_008397.1:g.104295_104325delinsGGAAAAAAACAATTTGCACATACCATATGTC

Transcript Alleles

HGVS Amino-acid change
ENST00000411819.2:c.3497_3504+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
ENST00000420813.6:c.3497_3504+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
ENST00000455383.6:c.3497_3504+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
ENST00000700004.2:c.3410_3417+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
ENST00000699999.1:n.4468_4475+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
ENST00000700000.1:c.2228_2235+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
ENST00000700002.1:c.3800_3807+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
ENST00000700003.1:c.1249_1256+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
ENST00000700004.1:c.2567_2574+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
ENST00000700005.1:n.2645_2652+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
ENST00000700006.1:n.4952_4959+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
ENST00000700007.1:n.2389_2396+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
ENST00000700008.1:n.1963_1993delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
ENST00000700009.1:n.2458_2465+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
ENST00000700010.1:n.1203_1210+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
ENST00000700011.1:n.3088_3095+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
ENST00000682451.1:n.4367_4397delinsGGAAAAAAACAATTTGCACATACCATATGTC (FBXO11)
ENST00000684712.1:n.4629_4659delinsGGAAAAAAACAATTTGCACATACCATATGTC (FBXO11)
ENST00000234420.11:c.3794_3801+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
ENST00000540021.6:c.3404_3411+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
ENST00000652107.1:c.3497_3504+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
ENST00000673637.1:c.3497_3504+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
ENST00000234420.9:c.3794_3801+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
ENST00000405808.5:c.169+1814_169+1844delinsGGAAAAAAACAATTTGCACATACCATATGTC (FBXO11) ENSP00000385127.1:n.169+1814_169+1844deli...
ENST00000434234.5:c.*124+1613_*124+1643delinsGGAAAAAAACAATTTGCACATACCATATGTC (FBXO11) ENSP00000402692.1:n.*124+1613_*124+1643de...
ENST00000445503.5:c.*3141_*3148+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
ENST00000538136.1:c.2888_2895+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
ENST00000540021.5:c.3404_3411+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
ENST00000614496.4:c.2888_2895+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
ENST00000622629.4:c.695_702+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
NM_000179.2:c.3794_3801+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC , LRG_219t1:c.3794_3801+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
NM_001281492.1:c.3404_3411+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
NM_001281493.1:c.2888_2895+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
NM_001281494.1:c.2888_2895+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
XM_005264271.1:c.3497_3504+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
XM_011532798.1:c.3611_3618+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
XM_011532799.1:c.3497_3504+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
XM_011532800.1:c.3497_3504+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
XM_024452819.1:c.3794_3824delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6) XP_024308587.1:p.Gly1265=
XM_024452820.1:c.3611_3641delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6) XP_024308588.1:p.Gly1204=
XM_024452821.1:c.3497_3527delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6) XP_024308589.1:p.Gly1166=
XM_024452822.1:c.2888_2918delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6) XP_024308590.1:p.Gly963=
NM_000179.3:c.3794_3801+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
NM_001281492.2:c.3404_3411+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
NM_001281493.2:c.2888_2895+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)
NM_001281494.2:c.2888_2895+23delinsGACATATGGTATGTGCAAATTGTTTTTTTCC (MSH6)