Canonical Allele Identifier: CA415257555

Gene: EMD

Linked Data

• MyVariant Identifiers: chrX:g.153608148T>A (hg19) ; chrX:g.154379788T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379788T>A , CM000685.2:g.154379788T>A	GRCh38
NC_000023.10:g.153608148T>A , CM000685.1:g.153608148T>A	GRCh37
NC_000023.9:g.153261342T>A	NCBI36
NG_008677.1:g.10353T>A , LRG_745:g.10353T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.181T>A	ENSP00000507245.1:p.Phe61Ile
ENST00000682478.1:n.157T>A
ENST00000683576.1:n.157T>A
ENST00000683627.1:c.181T>A	ENSP00000507533.1:p.Phe61Ile
ENST00000684082.1:c.181T>A	ENSP00000508266.1:p.Phe61Ile
ENST00000684633.1:n.153T>A
ENST00000684678.1:c.177T>A	ENSP00000507059.1:p.Ala59=
ENST00000369842.9:c.181T>A MANE Select	ENSP00000358857.4:p.Phe61Ile
ENST00000369835.3:c.83-154T>A	ENSP00000358850.3:n.83-154T>A
ENST00000369842.8:c.181T>A	ENSP00000358857.4:p.Phe61Ile
ENST00000428228.5:c.*86T>A	ENSP00000401081.1:n.*86T>A
ENST00000468294.5:n.141T>A
ENST00000485261.1:n.164-154T>A
ENST00000486738.5:n.325T>A
ENST00000492448.1:n.164T>A
ENST00000494443.5:n.238T>A
NM_000117.2:c.181T>A , LRG_745t1:c.181T>A	NP_000108.1:p.Phe61Ile
XM_024452349.1:c.-28T>A	XP_024308117.1:n.-28T>A
NM_000117.3:c.181T>A MANE Select	NP_000108.1:p.Phe61Ile