Canonical Allele Identifier: CA2014342570
Gene: EMG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6974416A= , CM000674.2:g.6974416A= GRCh38
NC_000012.11:g.7083578A= , CM000674.1:g.7083578A= GRCh37
NC_000012.10:g.6953839A= NCBI36
NG_021408.1:g.8636A=
NG_021408.2:g.8636A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000599672.6:c.246A= MANE Select ENSP00000470560.1:p.Glu82=
ENST00000261406.7:c.228A= ENSP00000476966.2:p.Glu76=
ENST00000539196.2:c.109A=
ENST00000599672.5:c.246A= ENSP00000470560.1:p.Glu82=
ENST00000607161.5:c.249A= ENSP00000480420.1:p.Glu83=
ENST00000611981.1:n.257A=
ENST00000620255.1:n.235A=
NM_006331.7:c.246A= NP_006322.4:p.Glu82=
XM_011520907.1:c.246A= XP_011519209.1:p.Glu82=
NM_001320049.1:c.246A= NP_001306978.1:p.Glu82=
NR_135131.1:n.389A=
NM_006331.8:c.246A= MANE Select NP_006322.4:p.Glu82=
NM_001320049.2:c.246A= NP_001306978.1:p.Glu82=
NR_135131.2:n.257A=