Canonical Allele Identifier: CA415258455

Gene: EMD

Linked Data

• MyVariant Identifiers: chrX:g.153609255T>G (hg19) ; chrX:g.154380895T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380895T>G , CM000685.2:g.154380895T>G	GRCh38
NC_000023.10:g.153609255T>G , CM000685.1:g.153609255T>G	GRCh37
NC_000023.9:g.153262449T>G	NCBI36
NG_008677.1:g.11460T>G , LRG_745:g.11460T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.463T>G	ENSP00000507245.1:p.Tyr155Asp
ENST00000682478.1:n.653T>G
ENST00000683576.1:n.653T>G
ENST00000683627.1:c.463T>G	ENSP00000507533.1:p.Tyr155Asp
ENST00000684082.1:c.420T>G	ENSP00000508266.1:n.420T>G
ENST00000684633.1:n.435T>G
ENST00000684678.1:c.459T>G	ENSP00000507059.1:n.459T>G
ENST00000369842.9:c.463T>G MANE Select	ENSP00000358857.4:p.Tyr155Asp
ENST00000369835.3:c.358T>G	ENSP00000358850.3:p.Tyr120Asp
ENST00000369842.8:c.463T>G	ENSP00000358857.4:p.Tyr155Asp
ENST00000428228.5:c.*368T>G	ENSP00000401081.1:n.*368T>G
ENST00000471965.1:n.252T>G
ENST00000485261.1:n.732T>G
ENST00000486738.5:n.900T>G
ENST00000492448.1:n.446T>G
NM_000117.2:c.463T>G , LRG_745t1:c.463T>G	NP_000108.1:p.Tyr155Asp
XM_024452349.1:c.469T>G	XP_024308117.1:p.Tyr157Asp
NM_000117.3:c.463T>G MANE Select	NP_000108.1:p.Tyr155Asp