Canonical Allele Identifier: CA2466663822
Gene: EMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154379692T= , CM000685.2:g.154379692T= GRCh38
NC_000023.10:g.153608052T= , CM000685.1:g.153608052T= GRCh37
NC_000023.9:g.153261246T= NCBI36
NG_008677.1:g.10257T= , LRG_745:g.10257T=

Transcript Alleles

HGVS Amino-acid change
ENST00000682114.1:c.85T= ENSP00000507245.1:p.Ser29=
ENST00000682478.1:n.61T=
ENST00000683576.1:n.61T=
ENST00000683627.1:c.85T= ENSP00000507533.1:p.Ser29=
ENST00000684082.1:c.85T= ENSP00000508266.1:p.Ser29=
ENST00000684633.1:n.57T=
ENST00000684678.1:c.81T= ENSP00000507059.1:p.Asp27=
ENST00000369842.9:c.85T= MANE Select ENSP00000358857.4:p.Ser29=
ENST00000369835.3:c.82+126T= ENSP00000358850.3:n.82+126T=
ENST00000369842.8:c.85T= ENSP00000358857.4:p.Ser29=
ENST00000428228.5:c.56T= ENSP00000401081.1:p.Ile19=
ENST00000468294.5:n.45T=
ENST00000485261.1:n.163+126T=
ENST00000486738.5:n.229T=
ENST00000492448.1:n.68T=
ENST00000494443.5:n.142T=
NM_000117.2:c.85T= , LRG_745t1:c.85T= NP_000108.1:p.Ser29=
XM_024452349.1:c.-124T= XP_024308117.1:n.-124T=
NM_000117.3:c.85T= MANE Select NP_000108.1:p.Ser29=