Canonical Allele Identifier: CA2014342547
Gene: EMG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6974367G= , CM000674.2:g.6974367G= GRCh38
NC_000012.11:g.7083529G= , CM000674.1:g.7083529G= GRCh37
NC_000012.10:g.6953790G= NCBI36
NG_021408.1:g.8587G=
NG_021408.2:g.8587G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000599672.6:c.197G= MANE Select ENSP00000470560.1:p.Cys66=
ENST00000261406.7:c.179G= ENSP00000476966.2:p.Cys60=
ENST00000539196.2:c.60G=
ENST00000599672.5:c.197G= ENSP00000470560.1:p.Cys66=
ENST00000607161.5:c.200G= ENSP00000480420.1:p.Cys67=
ENST00000611981.1:n.208G=
ENST00000620255.1:n.186G=
NM_006331.7:c.197G= NP_006322.4:p.Cys66=
XM_011520907.1:c.197G= XP_011519209.1:p.Cys66=
NM_001320049.1:c.197G= NP_001306978.1:p.Cys66=
NR_135131.1:n.340G=
NM_006331.8:c.197G= MANE Select NP_006322.4:p.Cys66=
NM_001320049.2:c.197G= NP_001306978.1:p.Cys66=
NR_135131.2:n.208G=