Canonical Allele Identifier: CA519278043

Gene: EMD

Linked Data

• MyVariant Identifiers: chrX:g.153608601T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380241T>C , CM000685.2:g.154380241T>C	GRCh38
NC_000023.10:g.153608601T>C , CM000685.1:g.153608601T>C	GRCh37
NC_000023.9:g.153261795T>C	NCBI36
NG_008677.1:g.10806T>C , LRG_745:g.10806T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.273T>C	ENSP00000507245.1:p.Asn91=
ENST00000682478.1:n.463T>C
ENST00000683576.1:n.463T>C
ENST00000683627.1:c.273T>C	ENSP00000507533.1:p.Asn91=
ENST00000684082.1:c.266-36T>C	ENSP00000508266.1:n.266-36T>C
ENST00000684633.1:n.245T>C
ENST00000684678.1:c.269T>C	ENSP00000507059.1:n.269T>C
ENST00000369842.9:c.273T>C MANE Select	ENSP00000358857.4:p.Asn91=
ENST00000369835.3:c.168T>C	ENSP00000358850.3:p.Asn56=
ENST00000369842.8:c.273T>C	ENSP00000358857.4:p.Asn91=
ENST00000428228.5:c.*178T>C	ENSP00000401081.1:n.*178T>C
ENST00000468294.5:n.233T>C
ENST00000485261.1:n.463T>C
ENST00000486738.5:n.631T>C
ENST00000492448.1:n.256T>C
ENST00000494443.5:n.544T>C
NM_000117.2:c.273T>C , LRG_745t1:c.273T>C	NP_000108.1:p.Asn91=
XM_024452349.1:c.279T>C	XP_024308117.1:p.Asn93=
NM_000117.3:c.273T>C MANE Select	NP_000108.1:p.Asn91=