Canonical Allele Identifier: CA519277776

Gene: EMD

Linked Data

• gnomAD v4: X-154379502-T-C
• MyVariant Identifiers: chrX:g.153607862T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379502T>C , CM000685.2:g.154379502T>C	GRCh38
NC_000023.10:g.153607862T>C , CM000685.1:g.153607862T>C	GRCh37
NC_000023.9:g.153261056T>C	NCBI36
NG_008677.1:g.10067T>C , LRG_745:g.10067T>C
NG_011506.1:g.145A>G
NG_011506.2:g.137A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.18T>C	ENSP00000507245.1:p.Asp6=
ENST00000683627.1:c.18T>C	ENSP00000507533.1:p.Asp6=
ENST00000684082.1:c.18T>C	ENSP00000508266.1:p.Asp6=
ENST00000684678.1:c.18T>C	ENSP00000507059.1:p.Asp6=
ENST00000369842.9:c.18T>C MANE Select	ENSP00000358857.4:p.Asp6=
ENST00000369835.3:c.18T>C	ENSP00000358850.3:p.Asp6=
ENST00000369842.8:c.18T>C	ENSP00000358857.4:p.Asp6=
ENST00000428228.5:c.18T>C	ENSP00000401081.1:p.Asp6=
ENST00000485261.1:n.99T>C
ENST00000486738.5:n.162T>C
ENST00000494443.5:n.75T>C
NM_000117.2:c.18T>C , LRG_745t1:c.18T>C	NP_000108.1:p.Asp6=
XM_024452349.1:c.-191T>C	XP_024308117.1:n.-191T>C
NM_000117.3:c.18T>C MANE Select	NP_000108.1:p.Asp6=