Canonical Allele Identifier: CA415257820

Gene: EMD

Linked Data

• MyVariant Identifiers: chrX:g.153608609A>T (hg19) ; chrX:g.154380249A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380249A>T , CM000685.2:g.154380249A>T	GRCh38
NC_000023.10:g.153608609A>T , CM000685.1:g.153608609A>T	GRCh37
NC_000023.9:g.153261803A>T	NCBI36
NG_008677.1:g.10814A>T , LRG_745:g.10814A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.281A>T	ENSP00000507245.1:p.Tyr94Phe
ENST00000682478.1:n.471A>T
ENST00000683576.1:n.471A>T
ENST00000683627.1:c.281A>T	ENSP00000507533.1:p.Tyr94Phe
ENST00000684082.1:c.266-28A>T	ENSP00000508266.1:n.266-28A>T
ENST00000684633.1:n.253A>T
ENST00000684678.1:c.277A>T	ENSP00000507059.1:n.277A>T
ENST00000369842.9:c.281A>T MANE Select	ENSP00000358857.4:p.Tyr94Phe
ENST00000369835.3:c.176A>T	ENSP00000358850.3:p.Tyr59Phe
ENST00000369842.8:c.281A>T	ENSP00000358857.4:p.Tyr94Phe
ENST00000428228.5:c.*186A>T	ENSP00000401081.1:n.*186A>T
ENST00000468294.5:n.241A>T
ENST00000485261.1:n.471A>T
ENST00000486738.5:n.639A>T
ENST00000492448.1:n.264A>T
ENST00000494443.5:n.552A>T
NM_000117.2:c.281A>T , LRG_745t1:c.281A>T	NP_000108.1:p.Tyr94Phe
XM_024452349.1:c.287A>T	XP_024308117.1:p.Tyr96Phe
NM_000117.3:c.281A>T MANE Select	NP_000108.1:p.Tyr94Phe