Canonical Allele Identifier: CA2824296190

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380700A>G , CM000685.2:g.154380700A>G	GRCh38
NC_000023.10:g.153609060A>G , CM000685.1:g.153609060A>G	GRCh37
NC_000023.9:g.153262254A>G	NCBI36
NG_008677.1:g.11265A>G , LRG_745:g.11265A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.400-53A>G	ENSP00000507245.1:n.400-53A>G
ENST00000682478.1:n.590-53A>G
ENST00000683576.1:n.590-53A>G
ENST00000683627.1:c.400-53A>G	ENSP00000507533.1:n.400-53A>G
ENST00000684082.1:c.357-53A>G	ENSP00000508266.1:n.357-53A>G
ENST00000684633.1:n.372-53A>G
ENST00000684678.1:c.396-53A>G	ENSP00000507059.1:n.396-53A>G
ENST00000369842.9:c.400-53A>G MANE Select	ENSP00000358857.4:n.400-53A>G
ENST00000369835.3:c.295-53A>G	ENSP00000358850.3:n.295-53A>G
ENST00000369842.8:c.400-53A>G	ENSP00000358857.4:n.400-53A>G
ENST00000428228.5:c.*305-53A>G	ENSP00000401081.1:n.*305-53A>G
ENST00000468294.5:n.360-53A>G
ENST00000471965.1:n.136A>G
ENST00000485261.1:n.590-53A>G
ENST00000486738.5:n.758-53A>G
ENST00000492448.1:n.383-53A>G
NM_000117.2:c.400-53A>G , LRG_745t1:c.400-53A>G	NP_000108.1:n.400-53A>G
XM_024452349.1:c.406-53A>G	XP_024308117.1:n.406-53A>G
NM_000117.3:c.400-53A>G MANE Select	NP_000108.1:n.400-53A>G