Canonical Allele Identifier: CA1993253480

Gene: MAML2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.96259013_96259015delinsACT , CM000673.2:g.96259013_96259015delinsACT	GRCh38
NC_000011.9:g.95992177_95992179delinsACT , CM000673.1:g.95992177_95992179delinsACT	GRCh37
NC_000011.8:g.95631825_95631827delinsACT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000524717.6:c.513+82368_513+82370delinsAGT MANE Select	ENSP00000434552.1:n.513+82368_513+82370delinsAGT
ENST00000524717.5:c.513+82368_513+82370delinsAGT	ENSP00000434552.1:n.513+82368_513+82370delinsAGT
NM_032427.3:c.513+82368_513+82370delinsAGT	NP_115803.1:n.513+82368_513+82370delinsAGT
XM_011543024.1:c.-172+83893_-172+83895delinsAGT	XP_011541326.1:n.-172+83893_-172+83895delinsAGT
XM_011543025.1:c.513+82368_513+82370delinsAGT	XP_011541327.1:n.513+82368_513+82370delinsAGT
XM_011543024.3:c.-172+83893_-172+83895delinsAGT	XP_011541326.1:n.-172+83893_-172+83895delinsAGT
XM_011543025.2:c.513+82368_513+82370delinsAGT	XP_011541327.1:n.513+82368_513+82370delinsAGT
NM_032427.4:c.513+82368_513+82370delinsAGT MANE Select	NP_115803.1:n.513+82368_513+82370delinsAGT