Canonical Allele Identifier: CA2695236994
Gene: EMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154379686_154379690del , CM000685.2:g.154379686_154379690del GRCh38
NC_000023.10:g.153608046_153608050del , CM000685.1:g.153608046_153608050del GRCh37
NC_000023.9:g.153261240_153261244del NCBI36
NG_008677.1:g.10251_10255del , LRG_745:g.10251_10255del

Transcript Alleles

HGVS Amino-acid change
ENST00000682114.1:c.83-4_83del
ENST00000682478.1:n.59-4_59del
ENST00000683576.1:n.59-4_59del
ENST00000683627.1:c.83-4_83del
ENST00000684082.1:c.83-4_83del
ENST00000684633.1:n.55-4_55del
ENST00000684678.1:c.79-4_79del
ENST00000369842.9:c.83-4_83del
ENST00000369835.3:c.82+120_82+124del ENSP00000358850.3:n.82+120_82+124del
ENST00000369842.8:c.83-4_83del
ENST00000428228.5:c.54-4_54del
ENST00000468294.5:n.43-4_43del
ENST00000485261.1:n.163+120_163+124del
ENST00000486738.5:n.227-4_227del
ENST00000492448.1:n.62_66del
ENST00000494443.5:n.140-4_140del
NM_000117.2:c.83-4_83del , LRG_745t1:c.83-4_83del
XM_024452349.1:c.-126-4_-126del
NM_000117.3:c.83-4_83del