Canonical Allele Identifier: CA415258347

Gene: EMD

Linked Data

• MyVariant Identifiers: chrX:g.153609159A>T (hg19) ; chrX:g.154380799A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380799A>T , CM000685.2:g.154380799A>T	GRCh38
NC_000023.10:g.153609159A>T , CM000685.1:g.153609159A>T	GRCh37
NC_000023.9:g.153262353A>T	NCBI36
NG_008677.1:g.11364A>T , LRG_745:g.11364A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.446A>T	ENSP00000507245.1:p.Asp149Val
ENST00000682478.1:n.636A>T
ENST00000683576.1:n.636A>T
ENST00000683627.1:c.446A>T	ENSP00000507533.1:p.Asp149Val
ENST00000684082.1:c.403A>T	ENSP00000508266.1:n.403A>T
ENST00000684633.1:n.418A>T
ENST00000684678.1:c.442A>T	ENSP00000507059.1:n.442A>T
ENST00000369842.9:c.446A>T MANE Select	ENSP00000358857.4:p.Asp149Val
ENST00000369835.3:c.341A>T	ENSP00000358850.3:p.Asp114Val
ENST00000369842.8:c.446A>T	ENSP00000358857.4:p.Asp149Val
ENST00000428228.5:c.*351A>T	ENSP00000401081.1:n.*351A>T
ENST00000468294.5:n.406A>T
ENST00000471965.1:n.235A>T
ENST00000485261.1:n.636A>T
ENST00000486738.5:n.804A>T
ENST00000492448.1:n.429A>T
NM_000117.2:c.446A>T , LRG_745t1:c.446A>T	NP_000108.1:p.Asp149Val
XM_024452349.1:c.452A>T	XP_024308117.1:p.Asp151Val
NM_000117.3:c.446A>T MANE Select	NP_000108.1:p.Asp149Val