Canonical Allele Identifier: CA2466664315
Gene: EMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154380800T= , CM000685.2:g.154380800T= GRCh38
NC_000023.10:g.153609160T= , CM000685.1:g.153609160T= GRCh37
NC_000023.9:g.153262354T= NCBI36
NG_008677.1:g.11365T= , LRG_745:g.11365T=

Transcript Alleles

HGVS Amino-acid change
ENST00000682114.1:c.447T= ENSP00000507245.1:p.Asp149=
ENST00000682478.1:n.637T=
ENST00000683576.1:n.637T=
ENST00000683627.1:c.447T= ENSP00000507533.1:p.Asp149=
ENST00000684082.1:c.404T= ENSP00000508266.1:n.404T=
ENST00000684633.1:n.419T=
ENST00000684678.1:c.443T= ENSP00000507059.1:n.443T=
ENST00000369842.9:c.447T= MANE Select ENSP00000358857.4:p.Asp149=
ENST00000369835.3:c.342T= ENSP00000358850.3:p.Asp114=
ENST00000369842.8:c.447T= ENSP00000358857.4:p.Asp149=
ENST00000428228.5:c.*352T= ENSP00000401081.1:n.*352T=
ENST00000468294.5:n.407T=
ENST00000471965.1:n.236T=
ENST00000485261.1:n.637T=
ENST00000486738.5:n.805T=
ENST00000492448.1:n.430T=
NM_000117.2:c.447T= , LRG_745t1:c.447T= NP_000108.1:p.Asp149=
XM_024452349.1:c.453T= XP_024308117.1:p.Asp151=
NM_000117.3:c.447T= MANE Select NP_000108.1:p.Asp149=