Canonical Allele Identifier: CA2430311504

Gene: MAGED2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.54809966C= , CM000685.2:g.54809966C=	GRCh38
NC_000023.10:g.54836399C= , CM000685.1:g.54836399C=	GRCh37
NC_000023.9:g.54853124C=	NCBI36
NG_012844.1:g.7229C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000375068.6:c.290C= MANE Select	ENSP00000364209.1:p.Ala97=
ENST00000218439.8:c.290C=	ENSP00000218439.4:p.Ala97=
ENST00000347546.8:c.236C=	ENSP00000336962.4:p.Ala79=
ENST00000375053.6:c.290C=	ENSP00000364193.2:p.Ala97=
ENST00000375058.5:c.290C=	ENSP00000364198.1:p.Ala97=
ENST00000375060.5:c.176C=	ENSP00000364200.1:p.Ala59=
ENST00000375068.5:c.290C=	ENSP00000364209.1:p.Ala97=
ENST00000396224.1:c.290C=	ENSP00000379526.1:p.Ala97=
ENST00000463787.5:n.123-152C=
ENST00000485483.1:n.525C=
ENST00000497484.1:n.433C=
ENST00000627068.2:c.176C=	ENSP00000486563.1:p.Ala59=
NM_014599.5:c.290C=	NP_055414.2:p.Ala97=
NM_177433.2:c.290C=	NP_803182.1:p.Ala97=
NM_201222.2:c.290C=	NP_957516.1:p.Ala97=
NM_177433.3:c.290C= MANE Select	NP_803182.1:p.Ala97=
NM_014599.6:c.290C=	NP_055414.2:p.Ala97=
NM_201222.3:c.290C=	NP_957516.1:p.Ala97=