Canonical Allele Identifier: CA415259136

Gene: EMD

Linked Data

• MyVariant Identifiers: chrX:g.153609452T>G (hg19) ; chrX:g.154381092T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154381092T>G , CM000685.2:g.154381092T>G	GRCh38
NC_000023.10:g.153609452T>G , CM000685.1:g.153609452T>G	GRCh37
NC_000023.9:g.153262646T>G	NCBI36
NG_008677.1:g.11657T>G , LRG_745:g.11657T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.572+88T>G	ENSP00000507245.1:n.572+88T>G
ENST00000682478.1:n.762+88T>G
ENST00000683576.1:n.850T>G
ENST00000683627.1:c.660T>G	ENSP00000507533.1:p.Asp220Glu
ENST00000684082.1:c.617T>G	ENSP00000508266.1:n.617T>G
ENST00000684633.1:n.632T>G
ENST00000684678.1:c.568+88T>G	ENSP00000507059.1:n.568+88T>G
ENST00000369842.9:c.660T>G MANE Select	ENSP00000358857.4:p.Asp220Glu
ENST00000369835.3:c.555T>G	ENSP00000358850.3:p.Asp185Glu
ENST00000369842.8:c.660T>G	ENSP00000358857.4:p.Asp220Glu
ENST00000428228.5:c.*565T>G	ENSP00000401081.1:n.*565T>G
ENST00000471965.1:n.449T>G
ENST00000486738.5:n.1097T>G
ENST00000492448.1:n.643T>G
NM_000117.2:c.660T>G , LRG_745t1:c.660T>G	NP_000108.1:p.Asp220Glu
XM_024452349.1:c.666T>G	XP_024308117.1:p.Asp222Glu
NM_000117.3:c.660T>G MANE Select	NP_000108.1:p.Asp220Glu