Canonical Allele Identifier: CA873317289

Gene: EMD

Linked Data

• dbSNP Id: rs1390310729
• MyVariant Identifiers: chrX:g.154379298C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379298C>T , CM000685.2:g.154379298C>T	GRCh38
NC_000023.10:g.153607658C>T , CM000685.1:g.153607658C>T	GRCh37
NC_000023.9:g.153260852C>T	NCBI36
NG_008677.1:g.9863C>T , LRG_745:g.9863C>T
NG_011506.1:g.349G>A
NG_011506.2:g.341G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000369842.9:c.-187C>T MANE Select	ENSP00000358857.4:n.-187C>T
ENST00000369835.3:c.-187C>T	ENSP00000358850.3:n.-187C>T
ENST00000369842.8:c.-187C>T	ENSP00000358857.4:n.-187C>T
NM_000117.2:c.-187C>T , LRG_745t1:c.-187C>T	NP_000108.1:n.-187C>T
XM_024452349.1:c.-395C>T	XP_024308117.1:n.-395C>T
NM_000117.3:c.-187C>T MANE Select	NP_000108.1:n.-187C>T