Canonical Allele Identifier: CA2466664348

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380869T= , CM000685.2:g.154380869T=	GRCh38
NC_000023.10:g.153609229T= , CM000685.1:g.153609229T=	GRCh37
NC_000023.9:g.153262423T=	NCBI36
NG_008677.1:g.11434T= , LRG_745:g.11434T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.450-13T=	ENSP00000507245.1:n.450-13T=
ENST00000682478.1:n.640-13T=
ENST00000683576.1:n.640-13T=
ENST00000683627.1:c.450-13T=	ENSP00000507533.1:n.450-13T=
ENST00000684082.1:c.407-13T=	ENSP00000508266.1:n.407-13T=
ENST00000684633.1:n.422-13T=
ENST00000684678.1:c.446-13T=	ENSP00000507059.1:n.446-13T=
ENST00000369842.9:c.450-13T= MANE Select	ENSP00000358857.4:n.450-13T=
ENST00000369835.3:c.345-13T=	ENSP00000358850.3:n.345-13T=
ENST00000369842.8:c.450-13T=	ENSP00000358857.4:n.450-13T=
ENST00000428228.5:c.*355-13T=	ENSP00000401081.1:n.*355-13T=
ENST00000468294.5:n.476T=
ENST00000471965.1:n.239-13T=
ENST00000485261.1:n.706T=
ENST00000486738.5:n.874T=
ENST00000492448.1:n.433-13T=
NM_000117.2:c.450-13T= , LRG_745t1:c.450-13T=	NP_000108.1:n.450-13T=
XM_024452349.1:c.456-13T=	XP_024308117.1:n.456-13T=
NM_000117.3:c.450-13T= MANE Select	NP_000108.1:n.450-13T=