Canonical Allele Identifier: CA2014342634
Gene: EMG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6974522T= , CM000674.2:g.6974522T= GRCh38
NC_000012.11:g.7083684T= , CM000674.1:g.7083684T= GRCh37
NC_000012.10:g.6953945T= NCBI36
NG_021408.1:g.8742T=
NG_021408.2:g.8742T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000599672.6:c.271-30T= MANE Select ENSP00000470560.1:n.271-30T=
ENST00000261406.7:c.253-30T= ENSP00000476966.2:n.253-30T=
ENST00000539196.2:c.134-30T=
ENST00000599672.5:c.271-30T= ENSP00000470560.1:n.271-30T=
ENST00000607161.5:c.274-30T= ENSP00000480420.1:n.274-30T=
ENST00000611981.1:n.282-30T=
ENST00000620255.1:n.341T=
NM_006331.7:c.271-30T= NP_006322.4:n.271-30T=
XM_011520907.1:c.271-30T= XP_011519209.1:n.271-30T=
NM_001320049.1:c.271-30T= NP_001306978.1:n.271-30T=
NR_135131.1:n.414-30T=
NM_006331.8:c.271-30T= MANE Select NP_006322.4:n.271-30T=
NM_001320049.2:c.271-30T= NP_001306978.1:n.271-30T=
NR_135131.2:n.282-30T=