Canonical Allele Identifier: CA415257407

Gene: EMD

Linked Data

• MyVariant Identifiers: chrX:g.153608083T>C (hg19) ; chrX:g.154379723T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379723T>C , CM000685.2:g.154379723T>C	GRCh38
NC_000023.10:g.153608083T>C , CM000685.1:g.153608083T>C	GRCh37
NC_000023.9:g.153261277T>C	NCBI36
NG_008677.1:g.10288T>C , LRG_745:g.10288T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.116T>C	ENSP00000507245.1:p.Phe39Ser
ENST00000682478.1:n.92T>C
ENST00000683576.1:n.92T>C
ENST00000683627.1:c.116T>C	ENSP00000507533.1:p.Phe39Ser
ENST00000684082.1:c.116T>C	ENSP00000508266.1:p.Phe39Ser
ENST00000684633.1:n.88T>C
ENST00000684678.1:c.112T>C	ENSP00000507059.1:p.Ser38Pro
ENST00000369842.9:c.116T>C MANE Select	ENSP00000358857.4:p.Phe39Ser
ENST00000369835.3:c.82+157T>C	ENSP00000358850.3:n.82+157T>C
ENST00000369842.8:c.116T>C	ENSP00000358857.4:p.Phe39Ser
ENST00000428228.5:c.*21T>C	ENSP00000401081.1:n.*21T>C
ENST00000468294.5:n.76T>C
ENST00000485261.1:n.163+157T>C
ENST00000486738.5:n.260T>C
ENST00000492448.1:n.99T>C
ENST00000494443.5:n.173T>C
NM_000117.2:c.116T>C , LRG_745t1:c.116T>C	NP_000108.1:p.Phe39Ser
XM_024452349.1:c.-93T>C	XP_024308117.1:n.-93T>C
NM_000117.3:c.116T>C MANE Select	NP_000108.1:p.Phe39Ser