Canonical Allele Identifier: CA2466663771

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379595G= , CM000685.2:g.154379595G=	GRCh38
NC_000023.10:g.153607955G= , CM000685.1:g.153607955G=	GRCh37
NC_000023.9:g.153261149G=	NCBI36
NG_008677.1:g.10160G= , LRG_745:g.10160G=
NG_011506.1:g.52C=
NG_011506.2:g.44C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.82+29G=	ENSP00000507245.1:n.82+29G=
ENST00000682478.1:n.58+29G=
ENST00000683576.1:n.58+29G=
ENST00000683627.1:c.82+29G=	ENSP00000507533.1:n.82+29G=
ENST00000684082.1:c.82+29G=	ENSP00000508266.1:n.82+29G=
ENST00000684633.1:n.54+33G=
ENST00000684678.1:c.78+33G=	ENSP00000507059.1:n.78+33G=
ENST00000369842.9:c.82+29G= MANE Select	ENSP00000358857.4:n.82+29G=
ENST00000369835.3:c.82+29G=	ENSP00000358850.3:n.82+29G=
ENST00000369842.8:c.82+29G=	ENSP00000358857.4:n.82+29G=
ENST00000428228.5:c.53+58G=	ENSP00000401081.1:n.53+58G=
ENST00000468294.5:n.42+29G=
ENST00000485261.1:n.163+29G=
ENST00000486738.5:n.226+29G=
ENST00000494443.5:n.139+29G=
NM_000117.2:c.82+29G= , LRG_745t1:c.82+29G=	NP_000108.1:n.82+29G=
XM_024452349.1:c.-127+29G=	XP_024308117.1:n.-127+29G=
NM_000117.3:c.82+29G= MANE Select	NP_000108.1:n.82+29G=