Canonical Allele Identifier: CA2466663728

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379517G= , CM000685.2:g.154379517G=	GRCh38
NC_000023.10:g.153607877G= , CM000685.1:g.153607877G=	GRCh37
NC_000023.9:g.153261071G=	NCBI36
NG_008677.1:g.10082G= , LRG_745:g.10082G=
NG_011506.1:g.130C=
NG_011506.2:g.122C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.33G=	ENSP00000507245.1:p.Glu11=
ENST00000682478.1:n.9G=
ENST00000683576.1:n.9G=
ENST00000683627.1:c.33G=	ENSP00000507533.1:p.Glu11=
ENST00000684082.1:c.33G=	ENSP00000508266.1:p.Glu11=
ENST00000684633.1:n.9G=
ENST00000684678.1:c.33G=	ENSP00000507059.1:p.Glu11=
ENST00000369842.9:c.33G= MANE Select	ENSP00000358857.4:p.Glu11=
ENST00000369835.3:c.33G=	ENSP00000358850.3:p.Glu11=
ENST00000369842.8:c.33G=	ENSP00000358857.4:p.Glu11=
ENST00000428228.5:c.33G=	ENSP00000401081.1:p.Glu11=
ENST00000485261.1:n.114G=
ENST00000486738.5:n.177G=
ENST00000494443.5:n.90G=
NM_000117.2:c.33G= , LRG_745t1:c.33G=	NP_000108.1:p.Glu11=
XM_024452349.1:c.-176G=	XP_024308117.1:n.-176G=
NM_000117.3:c.33G= MANE Select	NP_000108.1:p.Glu11=