Canonical Allele Identifier: CA2466664214

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380580G= , CM000685.2:g.154380580G=	GRCh38
NC_000023.10:g.153608940G= , CM000685.1:g.153608940G=	GRCh37
NC_000023.9:g.153262134G=	NCBI36
NG_008677.1:g.11145G= , LRG_745:g.11145G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.400-173G=	ENSP00000507245.1:n.400-173G=
ENST00000682478.1:n.590-173G=
ENST00000683576.1:n.590-173G=
ENST00000683627.1:c.400-173G=	ENSP00000507533.1:n.400-173G=
ENST00000684082.1:c.357-173G=	ENSP00000508266.1:n.357-173G=
ENST00000684633.1:n.372-173G=
ENST00000684678.1:c.396-173G=	ENSP00000507059.1:n.396-173G=
ENST00000369842.9:c.400-173G= MANE Select	ENSP00000358857.4:n.400-173G=
ENST00000369835.3:c.295-173G=	ENSP00000358850.3:n.295-173G=
ENST00000369842.8:c.400-173G=	ENSP00000358857.4:n.400-173G=
ENST00000428228.5:c.*305-173G=	ENSP00000401081.1:n.*305-173G=
ENST00000468294.5:n.360-173G=
ENST00000471965.1:n.16G=
ENST00000485261.1:n.590-173G=
ENST00000486738.5:n.758-173G=
ENST00000492448.1:n.383-173G=
NM_000117.2:c.400-173G= , LRG_745t1:c.400-173G=	NP_000108.1:n.400-173G=
XM_024452349.1:c.406-173G=	XP_024308117.1:n.406-173G=
NM_000117.3:c.400-173G= MANE Select	NP_000108.1:n.400-173G=