Canonical Allele Identifier: CA121389
Gene: EMD HGNC NCBI

Linked Data

ClinVar Variation Id: 11179
ClinVar RCV Id: RCV000011929
dbSNP Id: rs104894806
MyVariant Identifiers: chrX:g.153609339C>A (hg19) chrX:g.154380979C>A (hg38)
PubMed: PMID:10323252 PMID:10382909
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154380979C>A , CM000685.2:g.154380979C>A GRCh38
NC_000023.10:g.153609339C>A , CM000685.1:g.153609339C>A GRCh37
NC_000023.9:g.153262533C>A NCBI36
NG_008677.1:g.11544C>A , LRG_745:g.11544C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000682114.1:c.547C>A ENSP00000507245.1:p.Pro183Thr
ENST00000682478.1:n.737C>A
ENST00000683576.1:n.737C>A
ENST00000683627.1:c.547C>A ENSP00000507533.1:p.Pro183Thr
ENST00000684082.1:c.504C>A ENSP00000508266.1:n.504C>A
ENST00000684633.1:n.519C>A
ENST00000684678.1:c.543C>A ENSP00000507059.1:n.543C>A
ENST00000369842.9:c.547C>A MANE Select ENSP00000358857.4:p.Pro183Thr
ENST00000369835.3:c.442C>A ENSP00000358850.3:p.Pro148Thr
ENST00000369842.8:c.547C>A ENSP00000358857.4:p.Pro183Thr
ENST00000428228.5:c.*452C>A ENSP00000401081.1:n.*452C>A
ENST00000471965.1:n.336C>A
ENST00000486738.5:n.984C>A
ENST00000492448.1:n.530C>A
NM_000117.2:c.547C>A , LRG_745t1:c.547C>A NP_000108.1:p.Pro183Thr
XM_024452349.1:c.553C>A XP_024308117.1:p.Pro185Thr
NM_000117.3:c.547C>A MANE Select NP_000108.1:p.Pro183Thr
Search 100 bp 5'
Search 100 bp 3'