Canonical Allele Identifier: CA415257284

Gene: EMD

Linked Data

• MyVariant Identifiers: chrX:g.153608055A>T (hg19) ; chrX:g.154379695A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379695A>T , CM000685.2:g.154379695A>T	GRCh38
NC_000023.10:g.153608055A>T , CM000685.1:g.153608055A>T	GRCh37
NC_000023.9:g.153261249A>T	NCBI36
NG_008677.1:g.10260A>T , LRG_745:g.10260A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.88A>T	ENSP00000507245.1:p.Thr30Ser
ENST00000682478.1:n.64A>T
ENST00000683576.1:n.64A>T
ENST00000683627.1:c.88A>T	ENSP00000507533.1:p.Thr30Ser
ENST00000684082.1:c.88A>T	ENSP00000508266.1:p.Thr30Ser
ENST00000684633.1:n.60A>T
ENST00000684678.1:c.84A>T	ENSP00000507059.1:p.Gln28His
ENST00000369842.9:c.88A>T MANE Select	ENSP00000358857.4:p.Thr30Ser
ENST00000369835.3:c.82+129A>T	ENSP00000358850.3:n.82+129A>T
ENST00000369842.8:c.88A>T	ENSP00000358857.4:p.Thr30Ser
ENST00000428228.5:c.59A>T	ENSP00000401081.1:p.Asn20Ile
ENST00000468294.5:n.48A>T
ENST00000485261.1:n.163+129A>T
ENST00000486738.5:n.232A>T
ENST00000492448.1:n.71A>T
ENST00000494443.5:n.145A>T
NM_000117.2:c.88A>T , LRG_745t1:c.88A>T	NP_000108.1:p.Thr30Ser
XM_024452349.1:c.-121A>T	XP_024308117.1:n.-121A>T
NM_000117.3:c.88A>T MANE Select	NP_000108.1:p.Thr30Ser