Canonical Allele Identifier: CA415257693

Gene: EMD

Linked Data

• MyVariant Identifiers: chrX:g.153608349A>T (hg19) ; chrX:g.154379989A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379989A>T , CM000685.2:g.154379989A>T	GRCh38
NC_000023.10:g.153608349A>T , CM000685.1:g.153608349A>T	GRCh37
NC_000023.9:g.153261543A>T	NCBI36
NG_008677.1:g.10554A>T , LRG_745:g.10554A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.235A>T	ENSP00000507245.1:p.Lys79Ter
ENST00000682478.1:n.211A>T
ENST00000683576.1:n.211A>T
ENST00000683627.1:c.235A>T	ENSP00000507533.1:p.Lys79Ter
ENST00000684082.1:c.235A>T	ENSP00000508266.1:p.Lys79Ter
ENST00000684633.1:n.207A>T
ENST00000684678.1:c.231A>T	ENSP00000507059.1:n.231A>T
ENST00000369842.9:c.235A>T MANE Select	ENSP00000358857.4:p.Lys79Ter
ENST00000369835.3:c.130A>T	ENSP00000358850.3:p.Lys44Ter
ENST00000369842.8:c.235A>T	ENSP00000358857.4:p.Lys79Ter
ENST00000428228.5:c.*140A>T	ENSP00000401081.1:n.*140A>T
ENST00000468294.5:n.195A>T
ENST00000485261.1:n.211A>T
ENST00000486738.5:n.379A>T
ENST00000492448.1:n.218A>T
ENST00000494443.5:n.292A>T
NM_000117.2:c.235A>T , LRG_745t1:c.235A>T	NP_000108.1:p.Lys79Ter
XM_024452349.1:c.27A>T	XP_024308117.1:p.Arg9Ser
NM_000117.3:c.235A>T MANE Select	NP_000108.1:p.Lys79Ter