Canonical Allele Identifier: CA415256892

Gene: EMD

Linked Data

• gnomAD v4: X-154379509-G-T
• MyVariant Identifiers: chrX:g.153607869G>T (hg19) ; chrX:g.154379509G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379509G>T , CM000685.2:g.154379509G>T	GRCh38
NC_000023.10:g.153607869G>T , CM000685.1:g.153607869G>T	GRCh37
NC_000023.9:g.153261063G>T	NCBI36
NG_008677.1:g.10074G>T , LRG_745:g.10074G>T
NG_011506.1:g.138C>A
NG_011506.2:g.130C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.25G>T	ENSP00000507245.1:p.Asp9Tyr
ENST00000682478.1:n.1G>T
ENST00000683576.1:n.1G>T
ENST00000683627.1:c.25G>T	ENSP00000507533.1:p.Asp9Tyr
ENST00000684082.1:c.25G>T	ENSP00000508266.1:p.Asp9Tyr
ENST00000684633.1:n.1G>T
ENST00000684678.1:c.25G>T	ENSP00000507059.1:p.Asp9Tyr
ENST00000369842.9:c.25G>T MANE Select	ENSP00000358857.4:p.Asp9Tyr
ENST00000369835.3:c.25G>T	ENSP00000358850.3:p.Asp9Tyr
ENST00000369842.8:c.25G>T	ENSP00000358857.4:p.Asp9Tyr
ENST00000428228.5:c.25G>T	ENSP00000401081.1:p.Asp9Tyr
ENST00000485261.1:n.106G>T
ENST00000486738.5:n.169G>T
ENST00000494443.5:n.82G>T
NM_000117.2:c.25G>T , LRG_745t1:c.25G>T	NP_000108.1:p.Asp9Tyr
XM_024452349.1:c.-184G>T	XP_024308117.1:n.-184G>T
NM_000117.3:c.25G>T MANE Select	NP_000108.1:p.Asp9Tyr