Canonical Allele Identifier: CA2695115251

Gene: EMD

Linked Data

• gnomAD v4: X-154380528-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380528T>G , CM000685.2:g.154380528T>G	GRCh38
NC_000023.10:g.153608888T>G , CM000685.1:g.153608888T>G	GRCh37
NC_000023.9:g.153262082T>G	NCBI36
NG_008677.1:g.11093T>G , LRG_745:g.11093T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.399+161T>G	ENSP00000507245.1:n.399+161T>G
ENST00000682478.1:n.589+161T>G
ENST00000683576.1:n.589+161T>G
ENST00000683627.1:c.399+161T>G	ENSP00000507533.1:n.399+161T>G
ENST00000684082.1:c.356+161T>G	ENSP00000508266.1:n.356+161T>G
ENST00000684633.1:n.371+161T>G
ENST00000684678.1:c.395+161T>G	ENSP00000507059.1:n.395+161T>G
ENST00000369842.9:c.399+161T>G MANE Select	ENSP00000358857.4:n.399+161T>G
ENST00000369835.3:c.294+161T>G	ENSP00000358850.3:n.294+161T>G
ENST00000369842.8:c.399+161T>G	ENSP00000358857.4:n.399+161T>G
ENST00000428228.5:c.*304+161T>G	ENSP00000401081.1:n.*304+161T>G
ENST00000468294.5:n.359+161T>G
ENST00000485261.1:n.589+161T>G
ENST00000486738.5:n.757+161T>G
ENST00000492448.1:n.382+161T>G
NM_000117.2:c.399+161T>G , LRG_745t1:c.399+161T>G	NP_000108.1:n.399+161T>G
XM_024452349.1:c.405+161T>G	XP_024308117.1:n.405+161T>G
NM_000117.3:c.399+161T>G MANE Select	NP_000108.1:n.399+161T>G