Canonical Allele Identifier: CA519709733

Gene: EMD

Linked Data

• MyVariant Identifiers: chrX:g.153609130T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380770T>G , CM000685.2:g.154380770T>G	GRCh38
NC_000023.10:g.153609130T>G , CM000685.1:g.153609130T>G	GRCh37
NC_000023.9:g.153262324T>G	NCBI36
NG_008677.1:g.11335T>G , LRG_745:g.11335T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.417T>G	ENSP00000507245.1:p.Leu139=
ENST00000682478.1:n.607T>G
ENST00000683576.1:n.607T>G
ENST00000683627.1:c.417T>G	ENSP00000507533.1:p.Leu139=
ENST00000684082.1:c.374T>G	ENSP00000508266.1:n.374T>G
ENST00000684633.1:n.389T>G
ENST00000684678.1:c.413T>G	ENSP00000507059.1:n.413T>G
ENST00000369842.9:c.417T>G MANE Select	ENSP00000358857.4:p.Leu139=
ENST00000369835.3:c.312T>G	ENSP00000358850.3:p.Leu104=
ENST00000369842.8:c.417T>G	ENSP00000358857.4:p.Leu139=
ENST00000428228.5:c.*322T>G	ENSP00000401081.1:n.*322T>G
ENST00000468294.5:n.377T>G
ENST00000471965.1:n.206T>G
ENST00000485261.1:n.607T>G
ENST00000486738.5:n.775T>G
ENST00000492448.1:n.400T>G
NM_000117.2:c.417T>G , LRG_745t1:c.417T>G	NP_000108.1:p.Leu139=
XM_024452349.1:c.423T>G	XP_024308117.1:p.Leu141=
NM_000117.3:c.417T>G MANE Select	NP_000108.1:p.Leu139=