Canonical Allele Identifier: CA2430312174

Gene: MAGED2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.54812151C= , CM000685.2:g.54812151C=	GRCh38
NC_000023.10:g.54838584C= , CM000685.1:g.54838584C=	GRCh37
NC_000023.9:g.54855309C=	NCBI36
NG_012844.1:g.9414C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375068.6:c.991-6C= MANE Select	ENSP00000364209.1:n.991-6C=
ENST00000218439.8:c.991-6C=	ENSP00000218439.4:n.991-6C=
ENST00000347546.8:c.937-6C=	ENSP00000336962.4:n.937-6C=
ENST00000375053.6:c.991-6C=	ENSP00000364193.2:n.991-6C=
ENST00000375058.5:c.991-6C=	ENSP00000364198.1:n.991-6C=
ENST00000375060.5:c.736-6C=	ENSP00000364200.1:n.736-6C=
ENST00000375068.5:c.991-6C=	ENSP00000364209.1:n.991-6C=
ENST00000396224.1:c.991-6C=	ENSP00000379526.1:n.991-6C=
ENST00000487482.5:n.123-6C=
ENST00000627068.2:c.736-6C=	ENSP00000486563.1:n.736-6C=
NM_014599.5:c.991-6C=	NP_055414.2:n.991-6C=
NM_177433.2:c.991-6C=	NP_803182.1:n.991-6C=
NM_201222.2:c.991-6C=	NP_957516.1:n.991-6C=
NM_177433.3:c.991-6C= MANE Select	NP_803182.1:n.991-6C=
NM_014599.6:c.991-6C=	NP_055414.2:n.991-6C=
NM_201222.3:c.991-6C=	NP_957516.1:n.991-6C=