Canonical Allele Identifier: CA415259051

Gene: EMD

Linked Data

• MyVariant Identifiers: chrX:g.153609420A>T (hg19) ; chrX:g.154381060A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154381060A>T , CM000685.2:g.154381060A>T	GRCh38
NC_000023.10:g.153609420A>T , CM000685.1:g.153609420A>T	GRCh37
NC_000023.9:g.153262614A>T	NCBI36
NG_008677.1:g.11625A>T , LRG_745:g.11625A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.572+56A>T	ENSP00000507245.1:n.572+56A>T
ENST00000682478.1:n.762+56A>T
ENST00000683576.1:n.818A>T
ENST00000683627.1:c.628A>T	ENSP00000507533.1:p.Asn210Tyr
ENST00000684082.1:c.585A>T	ENSP00000508266.1:n.585A>T
ENST00000684633.1:n.600A>T
ENST00000684678.1:c.568+56A>T	ENSP00000507059.1:n.568+56A>T
ENST00000369842.9:c.628A>T MANE Select	ENSP00000358857.4:p.Asn210Tyr
ENST00000369835.3:c.523A>T	ENSP00000358850.3:p.Asn175Tyr
ENST00000369842.8:c.628A>T	ENSP00000358857.4:p.Asn210Tyr
ENST00000428228.5:c.*533A>T	ENSP00000401081.1:n.*533A>T
ENST00000471965.1:n.417A>T
ENST00000486738.5:n.1065A>T
ENST00000492448.1:n.611A>T
NM_000117.2:c.628A>T , LRG_745t1:c.628A>T	NP_000108.1:p.Asn210Tyr
XM_024452349.1:c.634A>T	XP_024308117.1:p.Asn212Tyr
NM_000117.3:c.628A>T MANE Select	NP_000108.1:p.Asn210Tyr