Canonical Allele Identifier: CA2466664398
Gene: EMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154380974A= , CM000685.2:g.154380974A= GRCh38
NC_000023.10:g.153609334A= , CM000685.1:g.153609334A= GRCh37
NC_000023.9:g.153262528A= NCBI36
NG_008677.1:g.11539A= , LRG_745:g.11539A=

Transcript Alleles

HGVS Amino-acid change
ENST00000682114.1:c.542A= ENSP00000507245.1:p.Tyr181=
ENST00000682478.1:n.732A=
ENST00000683576.1:n.732A=
ENST00000683627.1:c.542A= ENSP00000507533.1:p.Tyr181=
ENST00000684082.1:c.499A= ENSP00000508266.1:n.499A=
ENST00000684633.1:n.514A=
ENST00000684678.1:c.538A= ENSP00000507059.1:n.538A=
ENST00000369842.9:c.542A= MANE Select ENSP00000358857.4:p.Tyr181=
ENST00000369835.3:c.437A= ENSP00000358850.3:p.Tyr146=
ENST00000369842.8:c.542A= ENSP00000358857.4:p.Tyr181=
ENST00000428228.5:c.*447A= ENSP00000401081.1:n.*447A=
ENST00000471965.1:n.331A=
ENST00000486738.5:n.979A=
ENST00000492448.1:n.525A=
NM_000117.2:c.542A= , LRG_745t1:c.542A= NP_000108.1:p.Tyr181=
XM_024452349.1:c.548A= XP_024308117.1:p.Tyr183=
NM_000117.3:c.542A= MANE Select NP_000108.1:p.Tyr181=