Canonical Allele Identifier: CA2824296151

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379591T>G , CM000685.2:g.154379591T>G	GRCh38
NC_000023.10:g.153607951T>G , CM000685.1:g.153607951T>G	GRCh37
NC_000023.9:g.153261145T>G	NCBI36
NG_008677.1:g.10156T>G , LRG_745:g.10156T>G
NG_011506.1:g.56A>C
NG_011506.2:g.48A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.82+25T>G	ENSP00000507245.1:n.82+25T>G
ENST00000682478.1:n.58+25T>G
ENST00000683576.1:n.58+25T>G
ENST00000683627.1:c.82+25T>G	ENSP00000507533.1:n.82+25T>G
ENST00000684082.1:c.82+25T>G	ENSP00000508266.1:n.82+25T>G
ENST00000684633.1:n.54+29T>G
ENST00000684678.1:c.78+29T>G	ENSP00000507059.1:n.78+29T>G
ENST00000369842.9:c.82+25T>G MANE Select	ENSP00000358857.4:n.82+25T>G
ENST00000369835.3:c.82+25T>G	ENSP00000358850.3:n.82+25T>G
ENST00000369842.8:c.82+25T>G	ENSP00000358857.4:n.82+25T>G
ENST00000428228.5:c.53+54T>G	ENSP00000401081.1:n.53+54T>G
ENST00000468294.5:n.42+25T>G
ENST00000485261.1:n.163+25T>G
ENST00000486738.5:n.226+25T>G
ENST00000494443.5:n.139+25T>G
NM_000117.2:c.82+25T>G , LRG_745t1:c.82+25T>G	NP_000108.1:n.82+25T>G
XM_024452349.1:c.-127+25T>G	XP_024308117.1:n.-127+25T>G
NM_000117.3:c.82+25T>G MANE Select	NP_000108.1:n.82+25T>G