Canonical Allele Identifier: CA2014342616
Gene: EMG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6974497G= , CM000674.2:g.6974497G= GRCh38
NC_000012.11:g.7083659G= , CM000674.1:g.7083659G= GRCh37
NC_000012.10:g.6953920G= NCBI36
NG_021408.1:g.8717G=
NG_021408.2:g.8717G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000599672.6:c.271-55G= MANE Select ENSP00000470560.1:n.271-55G=
ENST00000261406.7:c.253-55G= ENSP00000476966.2:n.253-55G=
ENST00000539196.2:c.134-55G=
ENST00000599672.5:c.271-55G= ENSP00000470560.1:n.271-55G=
ENST00000607161.5:c.274-55G= ENSP00000480420.1:n.274-55G=
ENST00000611981.1:n.282-55G=
ENST00000620255.1:n.316G=
NM_006331.7:c.271-55G= NP_006322.4:n.271-55G=
XM_011520907.1:c.271-55G= XP_011519209.1:n.271-55G=
NM_001320049.1:c.271-55G= NP_001306978.1:n.271-55G=
NR_135131.1:n.414-55G=
NM_006331.8:c.271-55G= MANE Select NP_006322.4:n.271-55G=
NM_001320049.2:c.271-55G= NP_001306978.1:n.271-55G=
NR_135131.2:n.282-55G=