Canonical Allele Identifier: CA415257766

Gene: EMD

Linked Data

• MyVariant Identifiers: chrX:g.153608379G>A (hg19) ; chrX:g.154380019G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380019G>A , CM000685.2:g.154380019G>A	GRCh38
NC_000023.10:g.153608379G>A , CM000685.1:g.153608379G>A	GRCh37
NC_000023.9:g.153261573G>A	NCBI36
NG_008677.1:g.10584G>A , LRG_745:g.10584G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.265G>A	ENSP00000507245.1:p.Gly89Ser
ENST00000682478.1:n.241G>A
ENST00000683576.1:n.241G>A
ENST00000683627.1:c.265G>A	ENSP00000507533.1:p.Gly89Ser
ENST00000684082.1:c.265G>A	ENSP00000508266.1:p.Gly89Arg
ENST00000684633.1:n.237G>A
ENST00000684678.1:c.261G>A	ENSP00000507059.1:n.261G>A
ENST00000369842.9:c.265G>A MANE Select	ENSP00000358857.4:p.Gly89Ser
ENST00000369835.3:c.160G>A	ENSP00000358850.3:p.Gly54Ser
ENST00000369842.8:c.265G>A	ENSP00000358857.4:p.Gly89Ser
ENST00000428228.5:c.*170G>A	ENSP00000401081.1:n.*170G>A
ENST00000468294.5:n.225G>A
ENST00000485261.1:n.241G>A
ENST00000486738.5:n.409G>A
ENST00000492448.1:n.248G>A
ENST00000494443.5:n.322G>A
NM_000117.2:c.265G>A , LRG_745t1:c.265G>A	NP_000108.1:p.Gly89Ser
XM_024452349.1:c.57G>A	XP_024308117.1:p.Arg19=
NM_000117.3:c.265G>A MANE Select	NP_000108.1:p.Gly89Ser