Canonical Allele Identifier: CA519277778

Gene: EMD

Linked Data

• MyVariant Identifiers: chrX:g.153607865T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379505T>C , CM000685.2:g.154379505T>C	GRCh38
NC_000023.10:g.153607865T>C , CM000685.1:g.153607865T>C	GRCh37
NC_000023.9:g.153261059T>C	NCBI36
NG_008677.1:g.10070T>C , LRG_745:g.10070T>C
NG_011506.1:g.142A>G
NG_011506.2:g.134A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.21T>C	ENSP00000507245.1:p.Leu7=
ENST00000683627.1:c.21T>C	ENSP00000507533.1:p.Leu7=
ENST00000684082.1:c.21T>C	ENSP00000508266.1:p.Leu7=
ENST00000684678.1:c.21T>C	ENSP00000507059.1:p.Leu7=
ENST00000369842.9:c.21T>C MANE Select	ENSP00000358857.4:p.Leu7=
ENST00000369835.3:c.21T>C	ENSP00000358850.3:p.Leu7=
ENST00000369842.8:c.21T>C	ENSP00000358857.4:p.Leu7=
ENST00000428228.5:c.21T>C	ENSP00000401081.1:p.Leu7=
ENST00000485261.1:n.102T>C
ENST00000486738.5:n.165T>C
ENST00000494443.5:n.78T>C
NM_000117.2:c.21T>C , LRG_745t1:c.21T>C	NP_000108.1:p.Leu7=
XM_024452349.1:c.-188T>C	XP_024308117.1:n.-188T>C
NM_000117.3:c.21T>C MANE Select	NP_000108.1:p.Leu7=