Canonical Allele Identifier: CA415257046

Gene: EMD

Linked Data

• gnomAD v4: X-154379541-C-A
• MyVariant Identifiers: chrX:g.153607901C>A (hg19) ; chrX:g.154379541C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379541C>A , CM000685.2:g.154379541C>A	GRCh38
NC_000023.10:g.153607901C>A , CM000685.1:g.153607901C>A	GRCh37
NC_000023.9:g.153261095C>A	NCBI36
NG_008677.1:g.10106C>A , LRG_745:g.10106C>A
NG_011506.1:g.106G>T
NG_011506.2:g.98G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.57C>A	ENSP00000507245.1:p.Tyr19Ter
ENST00000682478.1:n.33C>A
ENST00000683576.1:n.33C>A
ENST00000683627.1:c.57C>A	ENSP00000507533.1:p.Tyr19Ter
ENST00000684082.1:c.57C>A	ENSP00000508266.1:p.Tyr19Ter
ENST00000684633.1:n.33C>A
ENST00000684678.1:c.57C>A	ENSP00000507059.1:p.Tyr19Ter
ENST00000369842.9:c.57C>A MANE Select	ENSP00000358857.4:p.Tyr19Ter
ENST00000369835.3:c.57C>A	ENSP00000358850.3:p.Tyr19Ter
ENST00000369842.8:c.57C>A	ENSP00000358857.4:p.Tyr19Ter
ENST00000428228.5:c.53+4C>A	ENSP00000401081.1:n.53+4C>A
ENST00000468294.5:n.17C>A
ENST00000485261.1:n.138C>A
ENST00000486738.5:n.201C>A
ENST00000494443.5:n.114C>A
NM_000117.2:c.57C>A , LRG_745t1:c.57C>A	NP_000108.1:p.Tyr19Ter
XM_024452349.1:c.-152C>A	XP_024308117.1:n.-152C>A
NM_000117.3:c.57C>A MANE Select	NP_000108.1:p.Tyr19Ter