Canonical Allele Identifier: CA519277783

Gene: EMD

Linked Data

• gnomAD v4: X-154379511-T-C
• MyVariant Identifiers: chrX:g.153607871T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379511T>C , CM000685.2:g.154379511T>C	GRCh38
NC_000023.10:g.153607871T>C , CM000685.1:g.153607871T>C	GRCh37
NC_000023.9:g.153261065T>C	NCBI36
NG_008677.1:g.10076T>C , LRG_745:g.10076T>C
NG_011506.1:g.136A>G
NG_011506.2:g.128A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.27T>C	ENSP00000507245.1:p.Asp9=
ENST00000682478.1:n.3T>C
ENST00000683576.1:n.3T>C
ENST00000683627.1:c.27T>C	ENSP00000507533.1:p.Asp9=
ENST00000684082.1:c.27T>C	ENSP00000508266.1:p.Asp9=
ENST00000684633.1:n.3T>C
ENST00000684678.1:c.27T>C	ENSP00000507059.1:p.Asp9=
ENST00000369842.9:c.27T>C MANE Select	ENSP00000358857.4:p.Asp9=
ENST00000369835.3:c.27T>C	ENSP00000358850.3:p.Asp9=
ENST00000369842.8:c.27T>C	ENSP00000358857.4:p.Asp9=
ENST00000428228.5:c.27T>C	ENSP00000401081.1:p.Asp9=
ENST00000485261.1:n.108T>C
ENST00000486738.5:n.171T>C
ENST00000494443.5:n.84T>C
NM_000117.2:c.27T>C , LRG_745t1:c.27T>C	NP_000108.1:p.Asp9=
XM_024452349.1:c.-182T>C	XP_024308117.1:n.-182T>C
NM_000117.3:c.27T>C MANE Select	NP_000108.1:p.Asp9=