Canonical Allele Identifier: CA918946179

Gene: MAML2

Linked Data

• dbSNP Id: rs1591100788

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.96258982del , CM000673.2:g.96258982del	GRCh38
NC_000011.9:g.95992146del , CM000673.1:g.95992146del	GRCh37
NC_000011.8:g.95631794del	NCBI36

Transcript Alleles

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