Canonical Allele Identifier: CA2466664272

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380724A= , CM000685.2:g.154380724A=	GRCh38
NC_000023.10:g.153609084A= , CM000685.1:g.153609084A=	GRCh37
NC_000023.9:g.153262278A=	NCBI36
NG_008677.1:g.11289A= , LRG_745:g.11289A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.400-29A=	ENSP00000507245.1:n.400-29A=
ENST00000682478.1:n.590-29A=
ENST00000683576.1:n.590-29A=
ENST00000683627.1:c.400-29A=	ENSP00000507533.1:n.400-29A=
ENST00000684082.1:c.357-29A=	ENSP00000508266.1:n.357-29A=
ENST00000684633.1:n.372-29A=
ENST00000684678.1:c.396-29A=	ENSP00000507059.1:n.396-29A=
ENST00000369842.9:c.400-29A= MANE Select	ENSP00000358857.4:n.400-29A=
ENST00000369835.3:c.295-29A=	ENSP00000358850.3:n.295-29A=
ENST00000369842.8:c.400-29A=	ENSP00000358857.4:n.400-29A=
ENST00000428228.5:c.*305-29A=	ENSP00000401081.1:n.*305-29A=
ENST00000468294.5:n.360-29A=
ENST00000471965.1:n.160A=
ENST00000485261.1:n.590-29A=
ENST00000486738.5:n.758-29A=
ENST00000492448.1:n.383-29A=
NM_000117.2:c.400-29A= , LRG_745t1:c.400-29A=	NP_000108.1:n.400-29A=
XM_024452349.1:c.406-29A=	XP_024308117.1:n.406-29A=
NM_000117.3:c.400-29A= MANE Select	NP_000108.1:n.400-29A=