Canonical Allele Identifier: CA2496048041

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47798645_47798650delinsAAGATA , CM000664.2:g.47798645_47798650delinsAAGATA GRCh38
NC_000002.11:g.48025784_48025789delinsAAGATA , CM000664.1:g.48025784_48025789delinsAAGATA GRCh37
NC_000002.10:g.47879288_47879293delinsAAGATA NCBI36
NG_007111.1:g.20499_20504delinsAAGATA , LRG_219:g.20499_20504delinsAAGATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000411819.2:c.365_370delinsAAGATA (MSH6) ENSP00000406248.2:p.Glu122=
ENST00000420813.6:c.365_370delinsAAGATA (MSH6) ENSP00000390382.2:p.Glu122=
ENST00000455383.6:c.365_370delinsAAGATA (MSH6) ENSP00000397484.2:p.Glu122=
ENST00000700004.2:c.662_667delinsAAGATA (MSH6) ENSP00000514752.2:p.Glu221=
ENST00000699999.1:n.746_751delinsAAGATA (MSH6)
ENST00000700000.1:c.662_667delinsAAGATA (MSH6) ENSP00000514749.1:p.Glu221=
ENST00000700002.1:c.668_673delinsAAGATA (MSH6) ENSP00000514750.1:p.Glu223=
ENST00000700003.1:c.627+2582_627+2587delinsAAGATA (MSH6) ENSP00000514751.1:n.627+2582_627+2587delinsAAGATA
ENST00000234420.11:c.662_667delinsAAGATA (MSH6) MANE Select ENSP00000234420.5:p.Glu221=
ENST00000540021.6:c.272_277delinsAAGATA (MSH6) ENSP00000446475.1:p.Glu91=
ENST00000652107.1:c.365_370delinsAAGATA (MSH6) ENSP00000498629.1:p.Glu122=
ENST00000673637.1:c.365_370delinsAAGATA (MSH6) ENSP00000501310.1:p.Glu122=
ENST00000673922.1:n.384_389delinsAAGATA (MSH6)
ENST00000234420.9:c.662_667delinsAAGATA (MSH6) ENSP00000234420.4:p.Glu221=
ENST00000405808.5:c.170-9210_170-9205delinsTATCTT (FBXO11) ENSP00000385127.1:n.170-9210_170-9205delinsTATCTT
ENST00000411819.1:c.365_370delinsAAGATA (MSH6) ENSP00000406248.1:p.Glu122=
ENST00000434234.5:c.*125-9210_*125-9205delinsTATCTT (FBXO11) ENSP00000402692.1:n.*125-9210_*125-9205delinsTATCTT
ENST00000445503.5:c.*9_*14delinsAAGATA (MSH6) ENSP00000405294.1:n.*9_*14delinsAAGATA
ENST00000456246.1:c.*150_*155delinsAAGATA (MSH6) ENSP00000410570.1:n.*150_*155delinsAAGATA
ENST00000538136.1:c.-245_-240delinsAAGATA (MSH6) ENSP00000438580.1:n.-245_-240delinsAAGATA
ENST00000540021.5:c.272_277delinsAAGATA (MSH6) ENSP00000446475.1:p.Glu91=
ENST00000614496.4:c.-245_-240delinsAAGATA (MSH6) ENSP00000477844.1:n.-245_-240delinsAAGATA
ENST00000616033.4:c.659_664delinsAAGATA (MSH6) ENSP00000480261.1:p.Glu220=
ENST00000622629.4:c.-2435_-2430delinsAAGATA (MSH6) ENSP00000482078.1:n.-2435_-2430delinsAAGATA
NM_000179.2:c.662_667delinsAAGATA , LRG_219t1:c.662_667delinsAAGATA (MSH6) NP_000170.1:p.Glu221=
NM_001281492.1:c.272_277delinsAAGATA (MSH6) NP_001268421.1:p.Glu91=
NM_001281493.1:c.-245_-240delinsAAGATA (MSH6) NP_001268422.1:n.-245_-240delinsAAGATA
NM_001281494.1:c.-245_-240delinsAAGATA (MSH6) NP_001268423.1:n.-245_-240delinsAAGATA
XM_005264271.1:c.365_370delinsAAGATA (MSH6) XP_005264328.1:p.Glu122=
XM_011532798.1:c.479_484delinsAAGATA (MSH6) XP_011531100.1:p.Glu160=
XM_011532799.1:c.365_370delinsAAGATA (MSH6) XP_011531101.1:p.Glu122=
XM_011532800.1:c.365_370delinsAAGATA (MSH6) XP_011531102.1:p.Glu122=
XM_024452819.1:c.662_667delinsAAGATA (MSH6) XP_024308587.1:p.Glu221=
XM_024452820.1:c.479_484delinsAAGATA (MSH6) XP_024308588.1:p.Glu160=
XM_024452821.1:c.365_370delinsAAGATA (MSH6) XP_024308589.1:p.Glu122=
XM_024452822.1:c.-245_-240delinsAAGATA (MSH6) XP_024308590.1:n.-245_-240delinsAAGATA
NM_000179.3:c.662_667delinsAAGATA (MSH6) MANE Select NP_000170.1:p.Glu221=
NM_001281492.2:c.272_277delinsAAGATA (MSH6) NP_001268421.1:p.Glu91=
NM_001281493.2:c.-245_-240delinsAAGATA (MSH6) NP_001268422.1:n.-245_-240delinsAAGATA
NM_001281494.2:c.-245_-240delinsAAGATA (MSH6) NP_001268423.1:n.-245_-240delinsAAGATA