Canonical Allele Identifier: CA519277862

Gene: EMD

Linked Data

• MyVariant Identifiers: chrX:g.153608066T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379706T>G , CM000685.2:g.154379706T>G	GRCh38
NC_000023.10:g.153608066T>G , CM000685.1:g.153608066T>G	GRCh37
NC_000023.9:g.153261260T>G	NCBI36
NG_008677.1:g.10271T>G , LRG_745:g.10271T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.99T>G	ENSP00000507245.1:p.Leu33=
ENST00000682478.1:n.75T>G
ENST00000683576.1:n.75T>G
ENST00000683627.1:c.99T>G	ENSP00000507533.1:p.Leu33=
ENST00000684082.1:c.99T>G	ENSP00000508266.1:p.Leu33=
ENST00000684633.1:n.71T>G
ENST00000684678.1:c.95T>G	ENSP00000507059.1:p.Phe32Cys
ENST00000369842.9:c.99T>G MANE Select	ENSP00000358857.4:p.Leu33=
ENST00000369835.3:c.82+140T>G	ENSP00000358850.3:n.82+140T>G
ENST00000369842.8:c.99T>G	ENSP00000358857.4:p.Leu33=
ENST00000428228.5:c.*4T>G	ENSP00000401081.1:n.*4T>G
ENST00000468294.5:n.59T>G
ENST00000485261.1:n.163+140T>G
ENST00000486738.5:n.243T>G
ENST00000492448.1:n.82T>G
ENST00000494443.5:n.156T>G
NM_000117.2:c.99T>G , LRG_745t1:c.99T>G	NP_000108.1:p.Leu33=
XM_024452349.1:c.-110T>G	XP_024308117.1:n.-110T>G
NM_000117.3:c.99T>G MANE Select	NP_000108.1:p.Leu33=