Canonical Allele Identifier: CA2466664027
Gene: EMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154380140T= , CM000685.2:g.154380140T= GRCh38
NC_000023.10:g.153608500T= , CM000685.1:g.153608500T= GRCh37
NC_000023.9:g.153261694T= NCBI36
NG_008677.1:g.10705T= , LRG_745:g.10705T=

Transcript Alleles

HGVS Amino-acid change
ENST00000682114.1:c.266-94T= ENSP00000507245.1:n.266-94T=
ENST00000682478.1:n.362T=
ENST00000683576.1:n.362T=
ENST00000683627.1:c.266-94T= ENSP00000507533.1:n.266-94T=
ENST00000684082.1:c.265+121T= ENSP00000508266.1:n.265+121T=
ENST00000684633.1:n.238-94T=
ENST00000684678.1:c.262-94T= ENSP00000507059.1:n.262-94T=
ENST00000369842.9:c.266-94T= MANE Select ENSP00000358857.4:n.266-94T=
ENST00000369835.3:c.161-94T= ENSP00000358850.3:n.161-94T=
ENST00000369842.8:c.266-94T= ENSP00000358857.4:n.266-94T=
ENST00000428228.5:c.*171-94T= ENSP00000401081.1:n.*171-94T=
ENST00000468294.5:n.226-94T=
ENST00000485261.1:n.362T=
ENST00000486738.5:n.530T=
ENST00000492448.1:n.249-94T=
ENST00000494443.5:n.443T=
NM_000117.2:c.266-94T= , LRG_745t1:c.266-94T= NP_000108.1:n.266-94T=
XM_024452349.1:c.178T= XP_024308117.1:p.Cys60=
NM_000117.3:c.266-94T= MANE Select NP_000108.1:n.266-94T=