Canonical Allele Identifier: CA519277965

Gene: EMD

Linked Data

• MyVariant Identifiers: chrX:g.153608351A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379991A>G , CM000685.2:g.154379991A>G	GRCh38
NC_000023.10:g.153608351A>G , CM000685.1:g.153608351A>G	GRCh37
NC_000023.9:g.153261545A>G	NCBI36
NG_008677.1:g.10556A>G , LRG_745:g.10556A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.237A>G	ENSP00000507245.1:p.Lys79=
ENST00000682478.1:n.213A>G
ENST00000683576.1:n.213A>G
ENST00000683627.1:c.237A>G	ENSP00000507533.1:p.Lys79=
ENST00000684082.1:c.237A>G	ENSP00000508266.1:p.Lys79=
ENST00000684633.1:n.209A>G
ENST00000684678.1:c.233A>G	ENSP00000507059.1:n.233A>G
ENST00000369842.9:c.237A>G MANE Select	ENSP00000358857.4:p.Lys79=
ENST00000369835.3:c.132A>G	ENSP00000358850.3:p.Lys44=
ENST00000369842.8:c.237A>G	ENSP00000358857.4:p.Lys79=
ENST00000428228.5:c.*142A>G	ENSP00000401081.1:n.*142A>G
ENST00000468294.5:n.197A>G
ENST00000485261.1:n.213A>G
ENST00000486738.5:n.381A>G
ENST00000492448.1:n.220A>G
ENST00000494443.5:n.294A>G
NM_000117.2:c.237A>G , LRG_745t1:c.237A>G	NP_000108.1:p.Lys79=
XM_024452349.1:c.29A>G	XP_024308117.1:p.Lys10Arg
NM_000117.3:c.237A>G MANE Select	NP_000108.1:p.Lys79=