Canonical Allele Identifier: CA415258433

Gene: EMD

Linked Data

• MyVariant Identifiers: chrX:g.153609250C>G (hg19) ; chrX:g.154380890C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380890C>G , CM000685.2:g.154380890C>G	GRCh38
NC_000023.10:g.153609250C>G , CM000685.1:g.153609250C>G	GRCh37
NC_000023.9:g.153262444C>G	NCBI36
NG_008677.1:g.11455C>G , LRG_745:g.11455C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.458C>G	ENSP00000507245.1:p.Pro153Arg
ENST00000682478.1:n.648C>G
ENST00000683576.1:n.648C>G
ENST00000683627.1:c.458C>G	ENSP00000507533.1:p.Pro153Arg
ENST00000684082.1:c.415C>G	ENSP00000508266.1:n.415C>G
ENST00000684633.1:n.430C>G
ENST00000684678.1:c.454C>G	ENSP00000507059.1:n.454C>G
ENST00000369842.9:c.458C>G MANE Select	ENSP00000358857.4:p.Pro153Arg
ENST00000369835.3:c.353C>G	ENSP00000358850.3:p.Pro118Arg
ENST00000369842.8:c.458C>G	ENSP00000358857.4:p.Pro153Arg
ENST00000428228.5:c.*363C>G	ENSP00000401081.1:n.*363C>G
ENST00000468294.5:n.497C>G
ENST00000471965.1:n.247C>G
ENST00000485261.1:n.727C>G
ENST00000486738.5:n.895C>G
ENST00000492448.1:n.441C>G
NM_000117.2:c.458C>G , LRG_745t1:c.458C>G	NP_000108.1:p.Pro153Arg
XM_024452349.1:c.464C>G	XP_024308117.1:p.Pro155Arg
NM_000117.3:c.458C>G MANE Select	NP_000108.1:p.Pro153Arg