Canonical Allele Identifier: CA2695115222

Gene: EMD

Linked Data

• gnomAD v4: X-154380486-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380486C>T , CM000685.2:g.154380486C>T	GRCh38
NC_000023.10:g.153608846C>T , CM000685.1:g.153608846C>T	GRCh37
NC_000023.9:g.153262040C>T	NCBI36
NG_008677.1:g.11051C>T , LRG_745:g.11051C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.399+119C>T	ENSP00000507245.1:n.399+119C>T
ENST00000682478.1:n.589+119C>T
ENST00000683576.1:n.589+119C>T
ENST00000683627.1:c.399+119C>T	ENSP00000507533.1:n.399+119C>T
ENST00000684082.1:c.356+119C>T	ENSP00000508266.1:n.356+119C>T
ENST00000684633.1:n.371+119C>T
ENST00000684678.1:c.395+119C>T	ENSP00000507059.1:n.395+119C>T
ENST00000369842.9:c.399+119C>T MANE Select	ENSP00000358857.4:n.399+119C>T
ENST00000369835.3:c.294+119C>T	ENSP00000358850.3:n.294+119C>T
ENST00000369842.8:c.399+119C>T	ENSP00000358857.4:n.399+119C>T
ENST00000428228.5:c.*304+119C>T	ENSP00000401081.1:n.*304+119C>T
ENST00000468294.5:n.359+119C>T
ENST00000485261.1:n.589+119C>T
ENST00000486738.5:n.757+119C>T
ENST00000492448.1:n.382+119C>T
NM_000117.2:c.399+119C>T , LRG_745t1:c.399+119C>T	NP_000108.1:n.399+119C>T
XM_024452349.1:c.405+119C>T	XP_024308117.1:n.405+119C>T
NM_000117.3:c.399+119C>T MANE Select	NP_000108.1:n.399+119C>T