Canonical Allele Identifier: CA337289435

Gene: EMD

Linked Data

• ClinVar Variation Id: 2964243
• ClinVar RCV Id: RCV003820345
• dbSNP Id: rs951717059
• gnomAD v4: X-154380030-G-T
• MyVariant Identifiers: chrX:g.154380030G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380030G>T , CM000685.2:g.154380030G>T	GRCh38
NC_000023.10:g.153608390G>T , CM000685.1:g.153608390G>T	GRCh37
NC_000023.9:g.153261584G>T	NCBI36
NG_008677.1:g.10595G>T , LRG_745:g.10595G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.265+11G>T	ENSP00000507245.1:n.265+11G>T
ENST00000682478.1:n.252G>T
ENST00000683576.1:n.252G>T
ENST00000683627.1:c.265+11G>T	ENSP00000507533.1:n.265+11G>T
ENST00000684082.1:c.265+11G>T	ENSP00000508266.1:n.265+11G>T
ENST00000684633.1:n.237+11G>T
ENST00000684678.1:c.261+11G>T	ENSP00000507059.1:n.261+11G>T
ENST00000369842.9:c.265+11G>T MANE Select	ENSP00000358857.4:n.265+11G>T
ENST00000369835.3:c.160+11G>T	ENSP00000358850.3:n.160+11G>T
ENST00000369842.8:c.265+11G>T	ENSP00000358857.4:n.265+11G>T
ENST00000428228.5:c.*170+11G>T	ENSP00000401081.1:n.*170+11G>T
ENST00000468294.5:n.225+11G>T
ENST00000485261.1:n.252G>T
ENST00000486738.5:n.420G>T
ENST00000492448.1:n.248+11G>T
ENST00000494443.5:n.333G>T
NM_000117.2:c.265+11G>T , LRG_745t1:c.265+11G>T	NP_000108.1:n.265+11G>T
XM_024452349.1:c.68G>T	XP_024308117.1:p.Gly23Val
NM_000117.3:c.265+11G>T MANE Select	NP_000108.1:n.265+11G>T