Canonical Allele Identifier: CA415258825

Gene: EMD

Linked Data

• MyVariant Identifiers: chrX:g.153609351T>A (hg19) ; chrX:g.154380991T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380991T>A , CM000685.2:g.154380991T>A	GRCh38
NC_000023.10:g.153609351T>A , CM000685.1:g.153609351T>A	GRCh37
NC_000023.9:g.153262545T>A	NCBI36
NG_008677.1:g.11556T>A , LRG_745:g.11556T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.559T>A	ENSP00000507245.1:p.Ser187Thr
ENST00000682478.1:n.749T>A
ENST00000683576.1:n.749T>A
ENST00000683627.1:c.559T>A	ENSP00000507533.1:p.Ser187Thr
ENST00000684082.1:c.516T>A	ENSP00000508266.1:n.516T>A
ENST00000684633.1:n.531T>A
ENST00000684678.1:c.555T>A	ENSP00000507059.1:n.555T>A
ENST00000369842.9:c.559T>A MANE Select	ENSP00000358857.4:p.Ser187Thr
ENST00000369835.3:c.454T>A	ENSP00000358850.3:p.Ser152Thr
ENST00000369842.8:c.559T>A	ENSP00000358857.4:p.Ser187Thr
ENST00000428228.5:c.*464T>A	ENSP00000401081.1:n.*464T>A
ENST00000471965.1:n.348T>A
ENST00000486738.5:n.996T>A
ENST00000492448.1:n.542T>A
NM_000117.2:c.559T>A , LRG_745t1:c.559T>A	NP_000108.1:p.Ser187Thr
XM_024452349.1:c.565T>A	XP_024308117.1:p.Ser189Thr
NM_000117.3:c.559T>A MANE Select	NP_000108.1:p.Ser187Thr