Canonical Allele Identifier: CA2466663826

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379710G= , CM000685.2:g.154379710G=	GRCh38
NC_000023.10:g.153608070G= , CM000685.1:g.153608070G=	GRCh37
NC_000023.9:g.153261264G=	NCBI36
NG_008677.1:g.10275G= , LRG_745:g.10275G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.103G=	ENSP00000507245.1:p.Glu35=
ENST00000682478.1:n.79G=
ENST00000683576.1:n.79G=
ENST00000683627.1:c.103G=	ENSP00000507533.1:p.Glu35=
ENST00000684082.1:c.103G=	ENSP00000508266.1:p.Glu35=
ENST00000684633.1:n.75G=
ENST00000684678.1:c.99G=	ENSP00000507059.1:p.Thr33=
ENST00000369842.9:c.103G= MANE Select	ENSP00000358857.4:p.Glu35=
ENST00000369835.3:c.82+144G=	ENSP00000358850.3:n.82+144G=
ENST00000369842.8:c.103G=	ENSP00000358857.4:p.Glu35=
ENST00000428228.5:c.*8G=	ENSP00000401081.1:n.*8G=
ENST00000468294.5:n.63G=
ENST00000485261.1:n.163+144G=
ENST00000486738.5:n.247G=
ENST00000492448.1:n.86G=
ENST00000494443.5:n.160G=
NM_000117.2:c.103G= , LRG_745t1:c.103G=	NP_000108.1:p.Glu35=
XM_024452349.1:c.-106G=	XP_024308117.1:n.-106G=
NM_000117.3:c.103G= MANE Select	NP_000108.1:p.Glu35=