Canonical Allele Identifier: CA415258845

Gene: EMD

Linked Data

• MyVariant Identifiers: chrX:g.153609357T>A (hg19) ; chrX:g.154380997T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380997T>A , CM000685.2:g.154380997T>A	GRCh38
NC_000023.10:g.153609357T>A , CM000685.1:g.153609357T>A	GRCh37
NC_000023.9:g.153262551T>A	NCBI36
NG_008677.1:g.11562T>A , LRG_745:g.11562T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.565T>A	ENSP00000507245.1:p.Ser189Thr
ENST00000682478.1:n.755T>A
ENST00000683576.1:n.755T>A
ENST00000683627.1:c.565T>A	ENSP00000507533.1:p.Ser189Thr
ENST00000684082.1:c.522T>A	ENSP00000508266.1:n.522T>A
ENST00000684633.1:n.537T>A
ENST00000684678.1:c.561T>A	ENSP00000507059.1:n.561T>A
ENST00000369842.9:c.565T>A MANE Select	ENSP00000358857.4:p.Ser189Thr
ENST00000369835.3:c.460T>A	ENSP00000358850.3:p.Ser154Thr
ENST00000369842.8:c.565T>A	ENSP00000358857.4:p.Ser189Thr
ENST00000428228.5:c.*470T>A	ENSP00000401081.1:n.*470T>A
ENST00000471965.1:n.354T>A
ENST00000486738.5:n.1002T>A
ENST00000492448.1:n.548T>A
NM_000117.2:c.565T>A , LRG_745t1:c.565T>A	NP_000108.1:p.Ser189Thr
XM_024452349.1:c.571T>A	XP_024308117.1:p.Ser191Thr
NM_000117.3:c.565T>A MANE Select	NP_000108.1:p.Ser189Thr