Canonical Allele Identifier: CA2466664270

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380721G= , CM000685.2:g.154380721G=	GRCh38
NC_000023.10:g.153609081G= , CM000685.1:g.153609081G=	GRCh37
NC_000023.9:g.153262275G=	NCBI36
NG_008677.1:g.11286G= , LRG_745:g.11286G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.400-32G=	ENSP00000507245.1:n.400-32G=
ENST00000682478.1:n.590-32G=
ENST00000683576.1:n.590-32G=
ENST00000683627.1:c.400-32G=	ENSP00000507533.1:n.400-32G=
ENST00000684082.1:c.357-32G=	ENSP00000508266.1:n.357-32G=
ENST00000684633.1:n.372-32G=
ENST00000684678.1:c.396-32G=	ENSP00000507059.1:n.396-32G=
ENST00000369842.9:c.400-32G= MANE Select	ENSP00000358857.4:n.400-32G=
ENST00000369835.3:c.295-32G=	ENSP00000358850.3:n.295-32G=
ENST00000369842.8:c.400-32G=	ENSP00000358857.4:n.400-32G=
ENST00000428228.5:c.*305-32G=	ENSP00000401081.1:n.*305-32G=
ENST00000468294.5:n.360-32G=
ENST00000471965.1:n.157G=
ENST00000485261.1:n.590-32G=
ENST00000486738.5:n.758-32G=
ENST00000492448.1:n.383-32G=
NM_000117.2:c.400-32G= , LRG_745t1:c.400-32G=	NP_000108.1:n.400-32G=
XM_024452349.1:c.406-32G=	XP_024308117.1:n.406-32G=
NM_000117.3:c.400-32G= MANE Select	NP_000108.1:n.400-32G=