Canonical Allele Identifier: CA2551709640
Gene: NMU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55601090_55601091insATTAACCCGTATTGCTAGCAACAACGGTAAAGTATTATTCGTTGGTACTAAACGCGCGGCTCAAGAAGCAGTACAAGCTGCAGCAT , CM000666.2:g.55601090_55601091insATTAACCCGTATTGCTAGCAACAACGGTAAAGTATTATTCGTTGGTACTAAACGCGCGGCTCAAGAAGCAGTACAAGCTGCAGCAT GRCh38
NC_000004.11:g.56467257_56467258insATTAACCCGTATTGCTAGCAACAACGGTAAAGTATTATTCGTTGGTACTAAACGCGCGGCTCAAGAAGCAGTACAAGCTGCAGCAT , CM000666.1:g.56467257_56467258insATTAACCCGTATTGCTAGCAACAACGGTAAAGTATTATTCGTTGGTACTAAACGCGCGGCTCAAGAAGCAGTACAAGCTGCAGCAT GRCh37
NC_000004.10:g.56162014_56162015insATTAACCCGTATTGCTAGCAACAACGGTAAAGTATTATTCGTTGGTACTAAACGCGCGGCTCAAGAAGCAGTACAAGCTGCAGCAT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000264218.7:c.436-516_436-515insATGCTGCAGCTTGTACTGCTTCTTGAGCCGCGCGTTTAGTACCAACGAATAATACTTTACCGTTGTTGCTAGCAATACGGGTTAAT MANE Select ENSP00000264218.3:n.436-516_436-515insATG...
ENST00000505262.5:c.355-516_355-515insATGCTGCAGCTTGTACTGCTTCTTGAGCCGCGCGTTTAGTACCAACGAATAATACTTTACCGTTGTTGCTAGCAATACGGGTTAAT ENSP00000424246.1:n.355-516_355-515insATG...
ENST00000507338.1:c.361-516_361-515insATGCTGCAGCTTGTACTGCTTCTTGAGCCGCGCGTTTAGTACCAACGAATAATACTTTACCGTTGTTGCTAGCAATACGGGTTAAT ENSP00000422870.1:n.361-516_361-515insATG...
ENST00000509371.1:n.200-516_200-515insATGCTGCAGCTTGTACTGCTTCTTGAGCCGCGCGTTTAGTACCAACGAATAATACTTTACCGTTGTTGCTAGCAATACGGGTTAAT
ENST00000511469.5:c.388-516_388-515insATGCTGCAGCTTGTACTGCTTCTTGAGCCGCGCGTTTAGTACCAACGAATAATACTTTACCGTTGTTGCTAGCAATACGGGTTAAT ENSP00000422399.1:n.388-516_388-515insATG...
ENST00000515325.5:n.428-516_428-515insATGCTGCAGCTTGTACTGCTTCTTGAGCCGCGCGTTTAGTACCAACGAATAATACTTTACCGTTGTTGCTAGCAATACGGGTTAAT
NM_001292045.1:c.388-516_388-515insATGCTGCAGCTTGTACTGCTTCTTGAGCCGCGCGTTTAGTACCAACGAATAATACTTTACCGTTGTTGCTAGCAATACGGGTTAAT NP_001278974.1:n.388-516_388-515insATGCTG...
NM_001292046.1:c.361-516_361-515insATGCTGCAGCTTGTACTGCTTCTTGAGCCGCGCGTTTAGTACCAACGAATAATACTTTACCGTTGTTGCTAGCAATACGGGTTAAT NP_001278975.1:n.361-516_361-515insATGCTG...
NM_006681.3:c.436-516_436-515insATGCTGCAGCTTGTACTGCTTCTTGAGCCGCGCGTTTAGTACCAACGAATAATACTTTACCGTTGTTGCTAGCAATACGGGTTAAT NP_006672.1:n.436-516_436-515insATGCTGCAG...
NR_120489.1:n.428-516_428-515insATGCTGCAGCTTGTACTGCTTCTTGAGCCGCGCGTTTAGTACCAACGAATAATACTTTACCGTTGTTGCTAGCAATACGGGTTAAT
XM_011534367.1:c.385-516_385-515insATGCTGCAGCTTGTACTGCTTCTTGAGCCGCGCGTTTAGTACCAACGAATAATACTTTACCGTTGTTGCTAGCAATACGGGTTAAT XP_011532669.1:n.385-516_385-515insATGCTG...
XM_011534368.1:c.334-516_334-515insATGCTGCAGCTTGTACTGCTTCTTGAGCCGCGCGTTTAGTACCAACGAATAATACTTTACCGTTGTTGCTAGCAATACGGGTTAAT XP_011532670.1:n.334-516_334-515insATGCTG...
XM_011534367.2:c.385-516_385-515insATGCTGCAGCTTGTACTGCTTCTTGAGCCGCGCGTTTAGTACCAACGAATAATACTTTACCGTTGTTGCTAGCAATACGGGTTAAT XP_011532669.1:n.385-516_385-515insATGCTG...
XM_011534368.3:c.334-516_334-515insATGCTGCAGCTTGTACTGCTTCTTGAGCCGCGCGTTTAGTACCAACGAATAATACTTTACCGTTGTTGCTAGCAATACGGGTTAAT XP_011532670.1:n.334-516_334-515insATGCTG...
NM_006681.4:c.436-516_436-515insATGCTGCAGCTTGTACTGCTTCTTGAGCCGCGCGTTTAGTACCAACGAATAATACTTTACCGTTGTTGCTAGCAATACGGGTTAAT MANE Select NP_006672.1:n.436-516_436-515insATGCTGCAG...
NM_001292045.2:c.388-516_388-515insATGCTGCAGCTTGTACTGCTTCTTGAGCCGCGCGTTTAGTACCAACGAATAATACTTTACCGTTGTTGCTAGCAATACGGGTTAAT NP_001278974.1:n.388-516_388-515insATGCTG...
NM_001292046.2:c.361-516_361-515insATGCTGCAGCTTGTACTGCTTCTTGAGCCGCGCGTTTAGTACCAACGAATAATACTTTACCGTTGTTGCTAGCAATACGGGTTAAT NP_001278975.1:n.361-516_361-515insATGCTG...
NR_120489.2:n.523-516_523-515insATGCTGCAGCTTGTACTGCTTCTTGAGCCGCGCGTTTAGTACCAACGAATAATACTTTACCGTTGTTGCTAGCAATACGGGTTAAT