Canonical Allele Identifier: CA519709703

Gene: EMD

Linked Data

• MyVariant Identifiers: chrX:g.153609118T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380758T>C , CM000685.2:g.154380758T>C	GRCh38
NC_000023.10:g.153609118T>C , CM000685.1:g.153609118T>C	GRCh37
NC_000023.9:g.153262312T>C	NCBI36
NG_008677.1:g.11323T>C , LRG_745:g.11323T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.405T>C	ENSP00000507245.1:p.His135=
ENST00000682478.1:n.595T>C
ENST00000683576.1:n.595T>C
ENST00000683627.1:c.405T>C	ENSP00000507533.1:p.His135=
ENST00000684082.1:c.362T>C	ENSP00000508266.1:n.362T>C
ENST00000684633.1:n.377T>C
ENST00000684678.1:c.401T>C	ENSP00000507059.1:n.401T>C
ENST00000369842.9:c.405T>C MANE Select	ENSP00000358857.4:p.His135=
ENST00000369835.3:c.300T>C	ENSP00000358850.3:p.His100=
ENST00000369842.8:c.405T>C	ENSP00000358857.4:p.His135=
ENST00000428228.5:c.*310T>C	ENSP00000401081.1:n.*310T>C
ENST00000468294.5:n.365T>C
ENST00000471965.1:n.194T>C
ENST00000485261.1:n.595T>C
ENST00000486738.5:n.763T>C
ENST00000492448.1:n.388T>C
NM_000117.2:c.405T>C , LRG_745t1:c.405T>C	NP_000108.1:p.His135=
XM_024452349.1:c.411T>C	XP_024308117.1:p.His137=
NM_000117.3:c.405T>C MANE Select	NP_000108.1:p.His135=