Canonical Allele Identifier: CA2466664308
Gene: EMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154380785A= , CM000685.2:g.154380785A= GRCh38
NC_000023.10:g.153609145A= , CM000685.1:g.153609145A= GRCh37
NC_000023.9:g.153262339A= NCBI36
NG_008677.1:g.11350A= , LRG_745:g.11350A=

Transcript Alleles

HGVS Amino-acid change
ENST00000682114.1:c.432A= ENSP00000507245.1:p.Glu144=
ENST00000682478.1:n.622A=
ENST00000683576.1:n.622A=
ENST00000683627.1:c.432A= ENSP00000507533.1:p.Glu144=
ENST00000684082.1:c.389A= ENSP00000508266.1:n.389A=
ENST00000684633.1:n.404A=
ENST00000684678.1:c.428A= ENSP00000507059.1:n.428A=
ENST00000369842.9:c.432A= MANE Select ENSP00000358857.4:p.Glu144=
ENST00000369835.3:c.327A= ENSP00000358850.3:p.Glu109=
ENST00000369842.8:c.432A= ENSP00000358857.4:p.Glu144=
ENST00000428228.5:c.*337A= ENSP00000401081.1:n.*337A=
ENST00000468294.5:n.392A=
ENST00000471965.1:n.221A=
ENST00000485261.1:n.622A=
ENST00000486738.5:n.790A=
ENST00000492448.1:n.415A=
NM_000117.2:c.432A= , LRG_745t1:c.432A= NP_000108.1:p.Glu144=
XM_024452349.1:c.438A= XP_024308117.1:p.Glu146=
NM_000117.3:c.432A= MANE Select NP_000108.1:p.Glu144=