Canonical Allele Identifier: CA1993253446

Gene: MAML2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.96258981_96258982delinsTG , CM000673.2:g.96258981_96258982delinsTG	GRCh38
NC_000011.9:g.95992145_95992146delinsTG , CM000673.1:g.95992145_95992146delinsTG	GRCh37
NC_000011.8:g.95631793_95631794delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524717.6:c.513+82401_513+82402delinsCA MANE Select	ENSP00000434552.1:n.513+82401_513+82402delinsCA
ENST00000524717.5:c.513+82401_513+82402delinsCA	ENSP00000434552.1:n.513+82401_513+82402delinsCA
NM_032427.3:c.513+82401_513+82402delinsCA	NP_115803.1:n.513+82401_513+82402delinsCA
XM_011543024.1:c.-172+83926_-172+83927delinsCA	XP_011541326.1:n.-172+83926_-172+83927delinsCA
XM_011543025.1:c.513+82401_513+82402delinsCA	XP_011541327.1:n.513+82401_513+82402delinsCA
XM_011543024.3:c.-172+83926_-172+83927delinsCA	XP_011541326.1:n.-172+83926_-172+83927delinsCA
XM_011543025.2:c.513+82401_513+82402delinsCA	XP_011541327.1:n.513+82401_513+82402delinsCA
NM_032427.4:c.513+82401_513+82402delinsCA MANE Select	NP_115803.1:n.513+82401_513+82402delinsCA