Canonical Allele Identifier: CA2430312973

Gene: MAGED2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.54814735A= , CM000685.2:g.54814735A=	GRCh38
NC_000023.10:g.54841168A= , CM000685.1:g.54841168A=	GRCh37
NC_000023.9:g.54857893A=	NCBI36
NG_012844.1:g.11998A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000375068.6:c.1346A= MANE Select	ENSP00000364209.1:p.Tyr449=
ENST00000218439.8:c.1346A=	ENSP00000218439.4:p.Tyr449=
ENST00000347546.8:c.1292A=	ENSP00000336962.4:p.Tyr431=
ENST00000375053.6:c.1346A=	ENSP00000364193.2:p.Tyr449=
ENST00000375058.5:c.1346A=	ENSP00000364198.1:p.Tyr449=
ENST00000375060.5:c.1091A=	ENSP00000364200.1:p.Tyr364=
ENST00000375068.5:c.1346A=	ENSP00000364209.1:p.Tyr449=
ENST00000396224.1:c.1346A=	ENSP00000379526.1:p.Tyr449=
ENST00000627068.2:c.1091A=	ENSP00000486563.1:p.Tyr364=
NM_014599.5:c.1346A=	NP_055414.2:p.Tyr449=
NM_177433.2:c.1346A=	NP_803182.1:p.Tyr449=
NM_201222.2:c.1346A=	NP_957516.1:p.Tyr449=
NM_177433.3:c.1346A= MANE Select	NP_803182.1:p.Tyr449=
NM_014599.6:c.1346A=	NP_055414.2:p.Tyr449=
NM_201222.3:c.1346A=	NP_957516.1:p.Tyr449=