Canonical Allele Identifier: CA2838377829

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31913351A>C , CM000664.2:g.31913351A>C GRCh38
NC_000002.11:g.32138420A>C , CM000664.1:g.32138420A>C GRCh37
NC_000002.10:g.31991924A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000404530.6:c.437+4575T>G (MEMO1) MANE Select ENSP00000385557.1:n.437+4575T>G
ENST00000295065.9:c.437+4575T>G (MEMO1) ENSP00000295065.4:n.437+4575T>G
ENST00000379383.7:c.446+4575T>G (MEMO1) ENSP00000368691.3:n.446+4575T>G
ENST00000404530.5:c.437+4575T>G (MEMO1) ENSP00000385557.1:n.437+4575T>G
ENST00000413686.1:n.607+4575T>G (MEMO1)
ENST00000422936.5:n.83-21217T>G (MEMO1)
ENST00000426310.6:c.368+4575T>G (MEMO1) ENSP00000400795.2:n.368+4575T>G
ENST00000446765.5:n.510+4575T>G (DPY30)
ENST00000490459.5:n.471+4575T>G (MEMO1)
NM_001137602.2:c.368+4575T>G (MEMO1) NP_001131074.1:n.368+4575T>G
NM_001301833.1:c.437+4575T>G (MEMO1) NP_001288762.1:n.437+4575T>G
NM_001301852.1:c.292+4575T>G (MEMO1) NP_001288781.1:n.292+4575T>G
NM_015955.3:c.437+4575T>G (MEMO1) NP_057039.1:n.437+4575T>G
NR_126032.1:n.854+4575T>G (MEMO1)
NR_126034.1:n.487+4575T>G (MEMO1)
XM_005264352.2:c.437+4575T>G (MEMO1) XP_005264409.1:n.437+4575T>G
XM_011532892.1:c.437+4575T>G (MEMO1) XP_011531194.1:n.437+4575T>G
XM_011532893.1:c.292+4575T>G (MEMO1) XP_011531195.1:n.292+4575T>G
XM_011532894.1:c.292+4575T>G (MEMO1) XP_011531196.1:n.292+4575T>G
XM_011532895.1:c.292+4575T>G (MEMO1) XP_011531197.1:n.292+4575T>G
XM_011532896.1:c.292+4575T>G (MEMO1) XP_011531198.1:n.292+4575T>G
XM_011532897.1:c.437+4575T>G (MEMO1) XP_011531199.1:n.437+4575T>G
XR_244937.2:n.454+4575T>G (MEMO1)
XM_011532892.2:c.437+4575T>G (MEMO1) XP_011531194.1:n.437+4575T>G
XM_011532896.2:c.292+4575T>G (MEMO1) XP_011531198.1:n.292+4575T>G
XM_017004255.1:c.437+4575T>G (MEMO1) XP_016859744.1:n.437+4575T>G
XM_024452943.1:c.368+4575T>G (MEMO1) XP_024308711.1:n.368+4575T>G
XM_024452944.1:c.292+4575T>G (MEMO1) XP_024308712.1:n.292+4575T>G
NM_001137602.3:c.368+4575T>G (MEMO1) NP_001131074.1:n.368+4575T>G
NM_001301833.3:c.437+4575T>G (MEMO1) NP_001288762.1:n.437+4575T>G
NM_001301852.3:c.292+4575T>G (MEMO1) NP_001288781.1:n.292+4575T>G
NM_001371912.1:c.557+4575T>G (MEMO1) NP_001358841.1:n.557+4575T>G
NM_001371913.1:c.464+4575T>G (MEMO1) NP_001358842.1:n.464+4575T>G
NM_001371914.1:c.437+4575T>G (MEMO1) NP_001358843.1:n.437+4575T>G
NM_001371915.1:c.437+4575T>G (MEMO1) NP_001358844.1:n.437+4575T>G
NM_001371916.1:c.368+4575T>G (MEMO1) NP_001358845.1:n.368+4575T>G
NM_001371917.1:c.292+4575T>G (MEMO1) NP_001358846.1:n.292+4575T>G
NM_001371918.1:c.292+4575T>G (MEMO1) NP_001358847.1:n.292+4575T>G
NM_001371920.1:c.144-21217T>G (MEMO1) NP_001358849.1:n.144-21217T>G
NM_001371921.1:c.256+4575T>G (MEMO1) NP_001358850.1:n.256+4575T>G
NM_015955.4:c.437+4575T>G (MEMO1) NP_057039.1:n.437+4575T>G
NR_126032.2:n.854+4575T>G (MEMO1)
NR_126034.3:n.443+4575T>G (MEMO1)
NR_163995.1:n.915+4575T>G (MEMO1)
NR_163996.1:n.521+4575T>G (MEMO1)
NR_163997.1:n.884+4575T>G (MEMO1)
NR_163998.1:n.521+4575T>G (MEMO1)
NM_001137602.4:c.368+4575T>G (MEMO1) NP_001131074.1:n.368+4575T>G
NM_001301833.4:c.437+4575T>G (MEMO1) MANE Select NP_001288762.1:n.437+4575T>G
NM_001301852.4:c.292+4575T>G (MEMO1) NP_001288781.1:n.292+4575T>G
NM_001371912.2:c.557+4575T>G (MEMO1) NP_001358841.1:n.557+4575T>G
NM_001371913.2:c.464+4575T>G (MEMO1) NP_001358842.1:n.464+4575T>G
NM_001371914.2:c.437+4575T>G (MEMO1) NP_001358843.1:n.437+4575T>G
NM_001371916.2:c.368+4575T>G (MEMO1) NP_001358845.1:n.368+4575T>G
NM_001371917.2:c.292+4575T>G (MEMO1) NP_001358846.1:n.292+4575T>G
NM_001371918.2:c.292+4575T>G (MEMO1) NP_001358847.1:n.292+4575T>G
NM_001371920.2:c.144-21217T>G (MEMO1) NP_001358849.1:n.144-21217T>G
NM_001371921.2:c.256+4575T>G (MEMO1) NP_001358850.1:n.256+4575T>G
NM_001385196.1:c.719+4575T>G (MEMO1) NP_001372125.1:n.719+4575T>G
NM_015955.5:c.437+4575T>G (MEMO1) NP_057039.1:n.437+4575T>G
NR_126032.3:n.1198+4575T>G (MEMO1)
NR_126034.4:n.443+4575T>G (MEMO1)
NR_163995.2:n.1229+4575T>G (MEMO1)
NR_163996.2:n.521+4575T>G (MEMO1)
NR_163997.2:n.1198+4575T>G (MEMO1)
NR_163998.2:n.521+4575T>G (MEMO1)