Canonical Allele Identifier: CA2695115165

Gene: EMD

Linked Data

• gnomAD v4: X-154380105-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380108del , CM000685.2:g.154380108del	GRCh38
NC_000023.10:g.153608468del , CM000685.1:g.153608468del	GRCh37
NC_000023.9:g.153261662del	NCBI36
NG_008677.1:g.10673del , LRG_745:g.10673del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.265+89del	ENSP00000507245.1:n.265+89del
ENST00000682478.1:n.330del
ENST00000683576.1:n.330del
ENST00000683627.1:c.265+89del	ENSP00000507533.1:n.265+89del
ENST00000684082.1:c.265+89del	ENSP00000508266.1:n.265+89del
ENST00000684633.1:n.237+89del
ENST00000684678.1:c.261+89del	ENSP00000507059.1:n.261+89del
ENST00000369842.9:c.265+89del MANE Select	ENSP00000358857.4:n.265+89del
ENST00000369835.3:c.160+89del	ENSP00000358850.3:n.160+89del
ENST00000369842.8:c.265+89del	ENSP00000358857.4:n.265+89del
ENST00000428228.5:c.*170+89del	ENSP00000401081.1:n.*170+89del
ENST00000468294.5:n.225+89del
ENST00000485261.1:n.330del
ENST00000486738.5:n.498del
ENST00000492448.1:n.248+89del
ENST00000494443.5:n.411del
NM_000117.2:c.265+89del , LRG_745t1:c.265+89del	NP_000108.1:n.265+89del
XM_024452349.1:c.146del	XP_024308117.1:p.Pro49GlnfsTer7
NM_000117.3:c.265+89del MANE Select	NP_000108.1:n.265+89del