Canonical Allele Identifier: CA2824296140

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379416del , CM000685.2:g.154379416del	GRCh38
NC_000023.10:g.153607776del , CM000685.1:g.153607776del	GRCh37
NC_000023.9:g.153260970del	NCBI36
NG_008677.1:g.9981del , LRG_745:g.9981del
NG_011506.1:g.231del
NG_011506.2:g.223del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369842.9:c.-69del MANE Select	ENSP00000358857.4:n.-69del
ENST00000369835.3:c.-69del	ENSP00000358850.3:n.-69del
ENST00000369842.8:c.-69del	ENSP00000358857.4:n.-69del
ENST00000428228.5:c.-69del	ENSP00000401081.1:n.-69del
ENST00000485261.1:n.13del
ENST00000486738.5:n.76del
NM_000117.2:c.-69del , LRG_745t1:c.-69del	NP_000108.1:n.-69del
XM_024452349.1:c.-277del	XP_024308117.1:n.-277del
NM_000117.3:c.-69del MANE Select	NP_000108.1:n.-69del