Canonical Allele Identifier: CA2505715869
Gene: MAML2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.96133449_96133450insTTA , CM000673.2:g.96133449_96133450insTTA GRCh38
NC_000011.9:g.95866613_95866614insTTA , CM000673.1:g.95866613_95866614insTTA GRCh37
NC_000011.8:g.95506261_95506262insTTA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000524717.6:c.514-39933_514-39932insTAA MANE Select ENSP00000434552.1:n.514-39933_514-39932in...
ENST00000524717.5:c.514-39933_514-39932insTAA ENSP00000434552.1:n.514-39933_514-39932in...
NM_032427.3:c.514-39933_514-39932insTAA NP_115803.1:n.514-39933_514-39932insTAA
XM_011543023.1:c.73-39933_73-39932insTAA XP_011541325.1:n.73-39933_73-39932insTAA
XM_011543024.1:c.-171-39933_-171-39932insTAA XP_011541326.1:n.-171-39933_-171-39932ins...
XM_011543025.1:c.514-39933_514-39932insTAA XP_011541327.1:n.514-39933_514-39932insTA...
XM_011543023.3:c.73-39933_73-39932insTAA XP_011541325.1:n.73-39933_73-39932insTAA
XM_011543024.3:c.-171-39933_-171-39932insTAA XP_011541326.1:n.-171-39933_-171-39932ins...
XM_011543025.2:c.514-39933_514-39932insTAA XP_011541327.1:n.514-39933_514-39932insTA...
NM_032427.4:c.514-39933_514-39932insTAA MANE Select NP_115803.1:n.514-39933_514-39932insTAA