Canonical Allele Identifier: CA415258786

Gene: EMD

Linked Data

• MyVariant Identifiers: chrX:g.153609339C>G (hg19) ; chrX:g.154380979C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.547C>G	ENSP00000507245.1:p.Pro183Ala
ENST00000682478.1:n.737C>G
ENST00000683576.1:n.737C>G
ENST00000683627.1:c.547C>G	ENSP00000507533.1:p.Pro183Ala
ENST00000684082.1:c.504C>G	ENSP00000508266.1:n.504C>G
ENST00000684633.1:n.519C>G
ENST00000684678.1:c.543C>G	ENSP00000507059.1:n.543C>G
ENST00000369842.9:c.547C>G MANE Select	ENSP00000358857.4:p.Pro183Ala
ENST00000369835.3:c.442C>G	ENSP00000358850.3:p.Pro148Ala
ENST00000369842.8:c.547C>G	ENSP00000358857.4:p.Pro183Ala
ENST00000428228.5:c.*452C>G	ENSP00000401081.1:n.*452C>G
ENST00000471965.1:n.336C>G
ENST00000486738.5:n.984C>G
ENST00000492448.1:n.530C>G
NM_000117.2:c.547C>G , LRG_745t1:c.547C>G	NP_000108.1:p.Pro183Ala
XM_024452349.1:c.553C>G	XP_024308117.1:p.Pro185Ala
NM_000117.3:c.547C>G MANE Select	NP_000108.1:p.Pro183Ala