Canonical Allele Identifier: CA1993253471

Gene: MAML2

Linked Data

• dbSNP Id: rs1862709807

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.96259005_96259007dup , CM000673.2:g.96259005_96259007dup	GRCh38
NC_000011.9:g.95992169_95992171dup , CM000673.1:g.95992169_95992171dup	GRCh37
NC_000011.8:g.95631817_95631819dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000524717.6:c.513+82377_513+82379dup MANE Select	ENSP00000434552.1:n.513+82377_513+82379dup
ENST00000524717.5:c.513+82377_513+82379dup	ENSP00000434552.1:n.513+82377_513+82379dup
NM_032427.3:c.513+82377_513+82379dup	NP_115803.1:n.513+82377_513+82379dup
XM_011543024.1:c.-172+83902_-172+83904dup	XP_011541326.1:n.-172+83902_-172+83904dup
XM_011543025.1:c.513+82377_513+82379dup	XP_011541327.1:n.513+82377_513+82379dup
XM_011543024.3:c.-172+83902_-172+83904dup	XP_011541326.1:n.-172+83902_-172+83904dup
XM_011543025.2:c.513+82377_513+82379dup	XP_011541327.1:n.513+82377_513+82379dup
NM_032427.4:c.513+82377_513+82379dup MANE Select	NP_115803.1:n.513+82377_513+82379dup