Canonical Allele Identifier: CA519709887

Gene: EMD

Linked Data

• MyVariant Identifiers: chrX:g.153609245A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380885A>G , CM000685.2:g.154380885A>G	GRCh38
NC_000023.10:g.153609245A>G , CM000685.1:g.153609245A>G	GRCh37
NC_000023.9:g.153262439A>G	NCBI36
NG_008677.1:g.11450A>G , LRG_745:g.11450A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.453A>G	ENSP00000507245.1:p.Glu151=
ENST00000682478.1:n.643A>G
ENST00000683576.1:n.643A>G
ENST00000683627.1:c.453A>G	ENSP00000507533.1:p.Glu151=
ENST00000684082.1:c.410A>G	ENSP00000508266.1:n.410A>G
ENST00000684633.1:n.425A>G
ENST00000684678.1:c.449A>G	ENSP00000507059.1:n.449A>G
ENST00000369842.9:c.453A>G MANE Select	ENSP00000358857.4:p.Glu151=
ENST00000369835.3:c.348A>G	ENSP00000358850.3:p.Glu116=
ENST00000369842.8:c.453A>G	ENSP00000358857.4:p.Glu151=
ENST00000428228.5:c.*358A>G	ENSP00000401081.1:n.*358A>G
ENST00000468294.5:n.492A>G
ENST00000471965.1:n.242A>G
ENST00000485261.1:n.722A>G
ENST00000486738.5:n.890A>G
ENST00000492448.1:n.436A>G
NM_000117.2:c.453A>G , LRG_745t1:c.453A>G	NP_000108.1:p.Glu151=
XM_024452349.1:c.459A>G	XP_024308117.1:p.Glu153=
NM_000117.3:c.453A>G MANE Select	NP_000108.1:p.Glu151=