Canonical Allele Identifier: CA519710035

Gene: EMD

Linked Data

• MyVariant Identifiers: chrX:g.153609344T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380984T>G , CM000685.2:g.154380984T>G	GRCh38
NC_000023.10:g.153609344T>G , CM000685.1:g.153609344T>G	GRCh37
NC_000023.9:g.153262538T>G	NCBI36
NG_008677.1:g.11549T>G , LRG_745:g.11549T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.552T>G	ENSP00000507245.1:p.Thr184=
ENST00000682478.1:n.742T>G
ENST00000683576.1:n.742T>G
ENST00000683627.1:c.552T>G	ENSP00000507533.1:p.Thr184=
ENST00000684082.1:c.509T>G	ENSP00000508266.1:n.509T>G
ENST00000684633.1:n.524T>G
ENST00000684678.1:c.548T>G	ENSP00000507059.1:n.548T>G
ENST00000369842.9:c.552T>G MANE Select	ENSP00000358857.4:p.Thr184=
ENST00000369835.3:c.447T>G	ENSP00000358850.3:p.Thr149=
ENST00000369842.8:c.552T>G	ENSP00000358857.4:p.Thr184=
ENST00000428228.5:c.*457T>G	ENSP00000401081.1:n.*457T>G
ENST00000471965.1:n.341T>G
ENST00000486738.5:n.989T>G
ENST00000492448.1:n.535T>G
NM_000117.2:c.552T>G , LRG_745t1:c.552T>G	NP_000108.1:p.Thr184=
XM_024452349.1:c.558T>G	XP_024308117.1:p.Thr186=
NM_000117.3:c.552T>G MANE Select	NP_000108.1:p.Thr184=