Canonical Allele Identifier: CA2496053994

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47806407_47806408delinsCT , CM000664.2:g.47806407_47806408delinsCT GRCh38
NC_000002.11:g.48033546_48033547delinsCT , CM000664.1:g.48033546_48033547delinsCT GRCh37
NC_000002.10:g.47887050_47887051delinsCT NCBI36
NG_007111.1:g.28261_28262delinsCT , LRG_219:g.28261_28262delinsCT
NG_008397.1:g.104268_104269delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000411819.2:c.3505-45_3505-44delinsCT (MSH6) ENSP00000406248.2:n.3505-45_3505-44delinsCT
ENST00000420813.6:c.3505-45_3505-44delinsCT (MSH6) ENSP00000390382.2:n.3505-45_3505-44delinsCT
ENST00000455383.6:c.3505-45_3505-44delinsCT (MSH6) ENSP00000397484.2:n.3505-45_3505-44delinsCT
ENST00000700004.2:c.3418-45_3418-44delinsCT (MSH6) ENSP00000514752.2:n.3418-45_3418-44delinsCT
ENST00000699999.1:n.4476-45_4476-44delinsCT (MSH6)
ENST00000700000.1:c.2236-45_2236-44delinsCT (MSH6) ENSP00000514749.1:n.2236-45_2236-44delinsCT
ENST00000700002.1:c.3808-45_3808-44delinsCT (MSH6) ENSP00000514750.1:n.3808-45_3808-44delinsCT
ENST00000700003.1:c.1257-45_1257-44delinsCT (MSH6) ENSP00000514751.1:n.1257-45_1257-44delinsCT
ENST00000700004.1:c.2575-45_2575-44delinsCT (MSH6) ENSP00000514752.1:n.2575-45_2575-44delinsCT
ENST00000700005.1:n.2653-45_2653-44delinsCT (MSH6)
ENST00000700006.1:n.4960-45_4960-44delinsCT (MSH6)
ENST00000700007.1:n.2397-45_2397-44delinsCT (MSH6)
ENST00000700008.1:n.2019_2020delinsCT (MSH6)
ENST00000700009.1:n.2466-45_2466-44delinsCT (MSH6)
ENST00000700010.1:n.1211-45_1211-44delinsCT (MSH6)
ENST00000700011.1:n.3096-45_3096-44delinsCT (MSH6)
ENST00000682451.1:n.4340_4341delinsAG (FBXO11)
ENST00000684712.1:n.4602_4603delinsAG (FBXO11)
ENST00000234420.11:c.3802-45_3802-44delinsCT (MSH6) MANE Select ENSP00000234420.5:n.3802-45_3802-44delinsCT
ENST00000540021.6:c.3412-45_3412-44delinsCT (MSH6) ENSP00000446475.1:n.3412-45_3412-44delinsCT
ENST00000652107.1:c.3505-45_3505-44delinsCT (MSH6) ENSP00000498629.1:n.3505-45_3505-44delinsCT
ENST00000673637.1:c.3505-45_3505-44delinsCT (MSH6) ENSP00000501310.1:n.3505-45_3505-44delinsCT
ENST00000234420.9:c.3802-45_3802-44delinsCT (MSH6) ENSP00000234420.4:n.3802-45_3802-44delinsCT
ENST00000405808.5:c.169+1787_169+1788delinsAG (FBXO11) ENSP00000385127.1:n.169+1787_169+1788delinsAG
ENST00000434234.5:c.*124+1586_*124+1587delinsAG (FBXO11) ENSP00000402692.1:n.*124+1586_*124+1587delinsAG
ENST00000445503.5:c.*3149-45_*3149-44delinsCT (MSH6) ENSP00000405294.1:n.*3149-45_*3149-44delinsCT
ENST00000538136.1:c.2896-45_2896-44delinsCT (MSH6) ENSP00000438580.1:n.2896-45_2896-44delinsCT
ENST00000540021.5:c.3412-45_3412-44delinsCT (MSH6) ENSP00000446475.1:n.3412-45_3412-44delinsCT
ENST00000614496.4:c.2896-45_2896-44delinsCT (MSH6) ENSP00000477844.1:n.2896-45_2896-44delinsCT
ENST00000622629.4:c.703-45_703-44delinsCT (MSH6) ENSP00000482078.1:n.703-45_703-44delinsCT
NM_000179.2:c.3802-45_3802-44delinsCT , LRG_219t1:c.3802-45_3802-44delinsCT (MSH6) NP_000170.1:n.3802-45_3802-44delinsCT
NM_001281492.1:c.3412-45_3412-44delinsCT (MSH6) NP_001268421.1:n.3412-45_3412-44delinsCT
NM_001281493.1:c.2896-45_2896-44delinsCT (MSH6) NP_001268422.1:n.2896-45_2896-44delinsCT
NM_001281494.1:c.2896-45_2896-44delinsCT (MSH6) NP_001268423.1:n.2896-45_2896-44delinsCT
XM_005264271.1:c.3505-45_3505-44delinsCT (MSH6) XP_005264328.1:n.3505-45_3505-44delinsCT
XM_011532798.1:c.3619-45_3619-44delinsCT (MSH6) XP_011531100.1:n.3619-45_3619-44delinsCT
XM_011532799.1:c.3505-45_3505-44delinsCT (MSH6) XP_011531101.1:n.3505-45_3505-44delinsCT
XM_011532800.1:c.3505-45_3505-44delinsCT (MSH6) XP_011531102.1:n.3505-45_3505-44delinsCT
XM_024452819.1:c.3850_3851delinsCT (MSH6) XP_024308587.1:p.Leu1284=
XM_024452820.1:c.3667_3668delinsCT (MSH6) XP_024308588.1:p.Leu1223=
XM_024452821.1:c.3553_3554delinsCT (MSH6) XP_024308589.1:p.Leu1185=
XM_024452822.1:c.2944_2945delinsCT (MSH6) XP_024308590.1:p.Leu982=
NM_000179.3:c.3802-45_3802-44delinsCT (MSH6) MANE Select NP_000170.1:n.3802-45_3802-44delinsCT
NM_001281492.2:c.3412-45_3412-44delinsCT (MSH6) NP_001268421.1:n.3412-45_3412-44delinsCT
NM_001281493.2:c.2896-45_2896-44delinsCT (MSH6) NP_001268422.1:n.2896-45_2896-44delinsCT
NM_001281494.2:c.2896-45_2896-44delinsCT (MSH6) NP_001268423.1:n.2896-45_2896-44delinsCT