Canonical Allele Identifier: CA2466663787

Gene: EMD

Linked Data

• dbSNP Id: rs2067874256

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379633_154379644dup , CM000685.2:g.154379633_154379644dup	GRCh38
NC_000023.10:g.153607993_153608004dup , CM000685.1:g.153607993_153608004dup	GRCh37
NC_000023.9:g.153261187_153261198dup	NCBI36
NG_008677.1:g.10198_10209dup , LRG_745:g.10198_10209dup
NG_011506.1:g.12_23dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.83-57_83-46dup	ENSP00000507245.1:n.83-57_83-46dup
ENST00000682478.1:n.59-57_59-46dup
ENST00000683576.1:n.59-57_59-46dup
ENST00000683627.1:c.83-57_83-46dup	ENSP00000507533.1:n.83-57_83-46dup
ENST00000684082.1:c.83-57_83-46dup	ENSP00000508266.1:n.83-57_83-46dup
ENST00000684633.1:n.55-57_55-46dup
ENST00000684678.1:c.79-57_79-46dup	ENSP00000507059.1:n.79-57_79-46dup
ENST00000369842.9:c.83-57_83-46dup MANE Select	ENSP00000358857.4:n.83-57_83-46dup
ENST00000369835.3:c.82+67_82+78dup	ENSP00000358850.3:n.82+67_82+78dup
ENST00000369842.8:c.83-57_83-46dup	ENSP00000358857.4:n.83-57_83-46dup
ENST00000428228.5:c.54-57_54-46dup	ENSP00000401081.1:n.54-57_54-46dup
ENST00000468294.5:n.43-57_43-46dup
ENST00000485261.1:n.163+67_163+78dup
ENST00000486738.5:n.227-57_227-46dup
ENST00000494443.5:n.140-57_140-46dup
NM_000117.2:c.83-57_83-46dup , LRG_745t1:c.83-57_83-46dup	NP_000108.1:n.83-57_83-46dup
XM_024452349.1:c.-126-57_-126-46dup	XP_024308117.1:n.-126-57_-126-46dup
NM_000117.3:c.83-57_83-46dup MANE Select	NP_000108.1:n.83-57_83-46dup