Canonical Allele Identifier: CA519277864

Gene: EMD

Linked Data

• ClinVar Variation Id: 2029537
• ClinVar RCV Id: RCV002863801
• MyVariant Identifiers: chrX:g.153608072G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379712G>A , CM000685.2:g.154379712G>A	GRCh38
NC_000023.10:g.153608072G>A , CM000685.1:g.153608072G>A	GRCh37
NC_000023.9:g.153261266G>A	NCBI36
NG_008677.1:g.10277G>A , LRG_745:g.10277G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.105G>A	ENSP00000507245.1:p.Glu35=
ENST00000682478.1:n.81G>A
ENST00000683576.1:n.81G>A
ENST00000683627.1:c.105G>A	ENSP00000507533.1:p.Glu35=
ENST00000684082.1:c.105G>A	ENSP00000508266.1:p.Glu35=
ENST00000684633.1:n.77G>A
ENST00000684678.1:c.101G>A	ENSP00000507059.1:p.Arg34Lys
ENST00000369842.9:c.105G>A MANE Select	ENSP00000358857.4:p.Glu35=
ENST00000369835.3:c.82+146G>A	ENSP00000358850.3:n.82+146G>A
ENST00000369842.8:c.105G>A	ENSP00000358857.4:p.Glu35=
ENST00000428228.5:c.*10G>A	ENSP00000401081.1:n.*10G>A
ENST00000468294.5:n.65G>A
ENST00000485261.1:n.163+146G>A
ENST00000486738.5:n.249G>A
ENST00000492448.1:n.88G>A
ENST00000494443.5:n.162G>A
NM_000117.2:c.105G>A , LRG_745t1:c.105G>A	NP_000108.1:p.Glu35=
XM_024452349.1:c.-104G>A	XP_024308117.1:n.-104G>A
NM_000117.3:c.105G>A MANE Select	NP_000108.1:p.Glu35=