Canonical Allele Identifier: CA2014342651
Gene: EMG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6974562T= , CM000674.2:g.6974562T= GRCh38
NC_000012.11:g.7083724T= , CM000674.1:g.7083724T= GRCh37
NC_000012.10:g.6953985T= NCBI36
NG_021408.1:g.8782T=
NG_021408.2:g.8782T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000599672.6:c.281T= MANE Select ENSP00000470560.1:p.Met94=
ENST00000261406.7:c.263T= ENSP00000476966.2:p.Met88=
ENST00000539196.2:c.144T=
ENST00000599672.5:c.281T= ENSP00000470560.1:p.Met94=
ENST00000607161.5:c.284T= ENSP00000480420.1:p.Met95=
ENST00000611981.1:n.292T=
ENST00000620255.1:n.381T=
NM_006331.7:c.281T= NP_006322.4:p.Met94=
XM_011520907.1:c.281T= XP_011519209.1:p.Met94=
NM_001320049.1:c.281T= NP_001306978.1:p.Met94=
NR_135131.1:n.424T=
NM_006331.8:c.281T= MANE Select NP_006322.4:p.Met94=
NM_001320049.2:c.281T= NP_001306978.1:p.Met94=
NR_135131.2:n.292T=