Canonical Allele Identifier: CA2695115178

Gene: EMD

Linked Data

• gnomAD v4: X-154380144-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380145del , CM000685.2:g.154380145del	GRCh38
NC_000023.10:g.153608505del , CM000685.1:g.153608505del	GRCh37
NC_000023.9:g.153261699del	NCBI36
NG_008677.1:g.10710del , LRG_745:g.10710del

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.266-89del	ENSP00000507245.1:n.266-89del
ENST00000682478.1:n.367del
ENST00000683576.1:n.367del
ENST00000683627.1:c.266-89del	ENSP00000507533.1:n.266-89del
ENST00000684082.1:c.265+126del	ENSP00000508266.1:n.265+126del
ENST00000684633.1:n.238-89del
ENST00000684678.1:c.262-89del	ENSP00000507059.1:n.262-89del
ENST00000369842.9:c.266-89del MANE Select	ENSP00000358857.4:n.266-89del
ENST00000369835.3:c.161-89del	ENSP00000358850.3:n.161-89del
ENST00000369842.8:c.266-89del	ENSP00000358857.4:n.266-89del
ENST00000428228.5:c.*171-89del	ENSP00000401081.1:n.*171-89del
ENST00000468294.5:n.226-89del
ENST00000485261.1:n.367del
ENST00000486738.5:n.535del
ENST00000492448.1:n.249-89del
ENST00000494443.5:n.448del
NM_000117.2:c.266-89del , LRG_745t1:c.266-89del	NP_000108.1:n.266-89del
XM_024452349.1:c.183del	XP_024308117.1:p.Tyr61Ter
NM_000117.3:c.266-89del MANE Select	NP_000108.1:n.266-89del