Canonical Allele Identifier: CA415258535

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380915C>G , CM000685.2:g.154380915C>G	GRCh38
NC_000023.10:g.153609275C>G , CM000685.1:g.153609275C>G	GRCh37
NC_000023.9:g.153262469C>G	NCBI36
NG_008677.1:g.11480C>G , LRG_745:g.11480C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000117.3:c.483C>G MANE Select	NP_000108.1:p.Tyr161Ter
ENST00000369842.9:c.483C>G MANE Select	ENSP00000358857.4:p.Tyr161Ter
NM_000117.2:c.483C>G , LRG_745t1:c.483C>G	NP_000108.1:p.Tyr161Ter
ENST00000369835.3:c.378C>G	ENSP00000358850.3:p.Tyr126Ter
ENST00000369842.8:c.483C>G	ENSP00000358857.4:p.Tyr161Ter
ENST00000428228.5:c.*388C>G	ENSP00000401081.1:n.*388C>G
ENST00000471965.1:n.272C>G
ENST00000485261.1:n.752C>G
ENST00000486738.5:n.920C>G
ENST00000492448.1:n.466C>G
ENST00000682114.1:c.483C>G	ENSP00000507245.1:p.Tyr161Ter
ENST00000682478.1:n.673C>G
ENST00000683576.1:n.673C>G
ENST00000683627.1:c.483C>G	ENSP00000507533.1:p.Tyr161Ter
ENST00000684082.1:c.440C>G	ENSP00000508266.1:n.440C>G
ENST00000684633.1:n.455C>G
ENST00000684678.1:c.479C>G	ENSP00000507059.1:n.479C>G
XM_024452349.1:c.489C>G	XP_024308117.1:p.Tyr163Ter