Canonical Allele Identifier: CA2014342542
Gene: EMG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6974356G= , CM000674.2:g.6974356G= GRCh38
NC_000012.11:g.7083518G= , CM000674.1:g.7083518G= GRCh37
NC_000012.10:g.6953779G= NCBI36
NG_021408.1:g.8576G=
NG_021408.2:g.8576G=

Transcript Alleles

HGVS Amino-acid change
ENST00000599672.6:c.186G= MANE Select ENSP00000470560.1:p.Glu62=
ENST00000261406.7:c.168G= ENSP00000476966.2:p.Glu56=
ENST00000539196.2:c.49G=
ENST00000599672.5:c.186G= ENSP00000470560.1:p.Glu62=
ENST00000607161.5:c.189G= ENSP00000480420.1:p.Glu63=
ENST00000611981.1:n.197G=
ENST00000620255.1:n.175G=
NM_006331.7:c.186G= NP_006322.4:p.Glu62=
XM_011520907.1:c.186G= XP_011519209.1:p.Glu62=
NM_001320049.1:c.186G= NP_001306978.1:p.Glu62=
NR_135131.1:n.329G=
NM_006331.8:c.186G= MANE Select NP_006322.4:p.Glu62=
NM_001320049.2:c.186G= NP_001306978.1:p.Glu62=
NR_135131.2:n.197G=