Canonical Allele Identifier: CA2466663710
Gene: EMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154379471A= , CM000685.2:g.154379471A= GRCh38
NC_000023.10:g.153607831A= , CM000685.1:g.153607831A= GRCh37
NC_000023.9:g.153261025A= NCBI36
NG_008677.1:g.10036A= , LRG_745:g.10036A=
NG_011506.1:g.176T=
NG_011506.2:g.168T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682114.1:c.-14A= ENSP00000507245.1:n.-14A=
ENST00000369842.9:c.-14A= MANE Select ENSP00000358857.4:n.-14A=
ENST00000369835.3:c.-14A= ENSP00000358850.3:n.-14A=
ENST00000369842.8:c.-14A= ENSP00000358857.4:n.-14A=
ENST00000428228.5:c.-14A= ENSP00000401081.1:n.-14A=
ENST00000485261.1:n.68A=
ENST00000486738.5:n.131A=
ENST00000494443.5:n.44A=
NM_000117.2:c.-14A= , LRG_745t1:c.-14A= NP_000108.1:n.-14A=
XM_024452349.1:c.-222A= XP_024308117.1:n.-222A=
NM_000117.3:c.-14A= MANE Select NP_000108.1:n.-14A=