Canonical Allele Identifier: CA2466663925

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379903_154379904delinsTG , CM000685.2:g.154379903_154379904delinsTG	GRCh38
NC_000023.10:g.153608263_153608264delinsTG , CM000685.1:g.153608263_153608264delinsTG	GRCh37
NC_000023.9:g.153261457_153261458delinsTG	NCBI36
NG_008677.1:g.10468_10469delinsTG , LRG_745:g.10468_10469delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.188-39_188-38delinsTG	ENSP00000507245.1:n.188-39_188-38delinsTG
ENST00000682478.1:n.164-39_164-38delinsTG
ENST00000683576.1:n.164-39_164-38delinsTG
ENST00000683627.1:c.188-39_188-38delinsTG	ENSP00000507533.1:n.188-39_188-38delinsTG
ENST00000684082.1:c.188-39_188-38delinsTG	ENSP00000508266.1:n.188-39_188-38delinsTG
ENST00000684633.1:n.160-39_160-38delinsTG
ENST00000684678.1:c.184-39_184-38delinsTG	ENSP00000507059.1:n.184-39_184-38delinsTG
ENST00000369842.9:c.188-39_188-38delinsTG MANE Select	ENSP00000358857.4:n.188-39_188-38delinsTG
ENST00000369835.3:c.83-39_83-38delinsTG	ENSP00000358850.3:n.83-39_83-38delinsTG
ENST00000369842.8:c.188-39_188-38delinsTG	ENSP00000358857.4:n.188-39_188-38delinsTG
ENST00000428228.5:c.*93-39_*93-38delinsTG	ENSP00000401081.1:n.*93-39_*93-38delinsTG
ENST00000468294.5:n.148-39_148-38delinsTG
ENST00000485261.1:n.164-39_164-38delinsTG
ENST00000486738.5:n.332-39_332-38delinsTG
ENST00000492448.1:n.171-39_171-38delinsTG
ENST00000494443.5:n.245-39_245-38delinsTG
NM_000117.2:c.188-39_188-38delinsTG , LRG_745t1:c.188-39_188-38delinsTG	NP_000108.1:n.188-39_188-38delinsTG
XM_024452349.1:c.-21-39_-21-38delinsTG	XP_024308117.1:n.-21-39_-21-38delinsTG
NM_000117.3:c.188-39_188-38delinsTG MANE Select	NP_000108.1:n.188-39_188-38delinsTG