Canonical Allele Identifier: CA415257308

Gene: EMD

Linked Data

• MyVariant Identifiers: chrX:g.153608061A>G (hg19) ; chrX:g.154379701A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379701A>G , CM000685.2:g.154379701A>G	GRCh38
NC_000023.10:g.153608061A>G , CM000685.1:g.153608061A>G	GRCh37
NC_000023.9:g.153261255A>G	NCBI36
NG_008677.1:g.10266A>G , LRG_745:g.10266A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.94A>G	ENSP00000507245.1:p.Arg32Gly
ENST00000682478.1:n.70A>G
ENST00000683576.1:n.70A>G
ENST00000683627.1:c.94A>G	ENSP00000507533.1:p.Arg32Gly
ENST00000684082.1:c.94A>G	ENSP00000508266.1:p.Arg32Gly
ENST00000684633.1:n.66A>G
ENST00000684678.1:c.90A>G	ENSP00000507059.1:p.Val30=
ENST00000369842.9:c.94A>G MANE Select	ENSP00000358857.4:p.Arg32Gly
ENST00000369835.3:c.82+135A>G	ENSP00000358850.3:n.82+135A>G
ENST00000369842.8:c.94A>G	ENSP00000358857.4:p.Arg32Gly
ENST00000428228.5:c.65A>G	ENSP00000401081.1:p.Ter22Trp
ENST00000468294.5:n.54A>G
ENST00000485261.1:n.163+135A>G
ENST00000486738.5:n.238A>G
ENST00000492448.1:n.77A>G
ENST00000494443.5:n.151A>G
NM_000117.2:c.94A>G , LRG_745t1:c.94A>G	NP_000108.1:p.Arg32Gly
XM_024452349.1:c.-115A>G	XP_024308117.1:n.-115A>G
NM_000117.3:c.94A>G MANE Select	NP_000108.1:p.Arg32Gly