Canonical Allele Identifier: CA2466663758

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379577G= , CM000685.2:g.154379577G=	GRCh38
NC_000023.10:g.153607937G= , CM000685.1:g.153607937G=	GRCh37
NC_000023.9:g.153261131G=	NCBI36
NG_008677.1:g.10142G= , LRG_745:g.10142G=
NG_011506.1:g.70C=
NG_011506.2:g.62C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.82+11G=	ENSP00000507245.1:n.82+11G=
ENST00000682478.1:n.58+11G=
ENST00000683576.1:n.58+11G=
ENST00000683627.1:c.82+11G=	ENSP00000507533.1:n.82+11G=
ENST00000684082.1:c.82+11G=	ENSP00000508266.1:n.82+11G=
ENST00000684633.1:n.54+15G=
ENST00000684678.1:c.78+15G=	ENSP00000507059.1:n.78+15G=
ENST00000369842.9:c.82+11G= MANE Select	ENSP00000358857.4:n.82+11G=
ENST00000369835.3:c.82+11G=	ENSP00000358850.3:n.82+11G=
ENST00000369842.8:c.82+11G=	ENSP00000358857.4:n.82+11G=
ENST00000428228.5:c.53+40G=	ENSP00000401081.1:n.53+40G=
ENST00000468294.5:n.42+11G=
ENST00000485261.1:n.163+11G=
ENST00000486738.5:n.226+11G=
ENST00000494443.5:n.139+11G=
NM_000117.2:c.82+11G= , LRG_745t1:c.82+11G=	NP_000108.1:n.82+11G=
XM_024452349.1:c.-127+11G=	XP_024308117.1:n.-127+11G=
NM_000117.3:c.82+11G= MANE Select	NP_000108.1:n.82+11G=