Canonical Allele Identifier: CA1993195821

Gene: MAML2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.96133603A= , CM000673.2:g.96133603A=	GRCh38
NC_000011.9:g.95866767A= , CM000673.1:g.95866767A=	GRCh37
NC_000011.8:g.95506415A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000524717.6:c.514-40086T= MANE Select	ENSP00000434552.1:n.514-40086T=
ENST00000524717.5:c.514-40086T=	ENSP00000434552.1:n.514-40086T=
NM_032427.3:c.514-40086T=	NP_115803.1:n.514-40086T=
XM_011543023.1:c.73-40086T=	XP_011541325.1:n.73-40086T=
XM_011543024.1:c.-171-40086T=	XP_011541326.1:n.-171-40086T=
XM_011543025.1:c.514-40086T=	XP_011541327.1:n.514-40086T=
XM_011543023.3:c.73-40086T=	XP_011541325.1:n.73-40086T=
XM_011543024.3:c.-171-40086T=	XP_011541326.1:n.-171-40086T=
XM_011543025.2:c.514-40086T=	XP_011541327.1:n.514-40086T=
NM_032427.4:c.514-40086T= MANE Select	NP_115803.1:n.514-40086T=