Canonical Allele Identifier: CA2014342537
Gene: EMG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6974346A= , CM000674.2:g.6974346A= GRCh38
NC_000012.11:g.7083508A= , CM000674.1:g.7083508A= GRCh37
NC_000012.10:g.6953769A= NCBI36
NG_021408.1:g.8566A=
NG_021408.2:g.8566A=

Transcript Alleles

HGVS Amino-acid change
ENST00000599672.6:c.176A= MANE Select ENSP00000470560.1:p.Lys59=
ENST00000261406.7:c.158A= ENSP00000476966.2:p.Lys53=
ENST00000539196.2:c.39A=
ENST00000599672.5:c.176A= ENSP00000470560.1:p.Lys59=
ENST00000607161.5:c.179A= ENSP00000480420.1:p.Lys60=
ENST00000611981.1:n.187A=
ENST00000620255.1:n.165A=
NM_006331.7:c.176A= NP_006322.4:p.Lys59=
XM_011520907.1:c.176A= XP_011519209.1:p.Lys59=
NM_001320049.1:c.176A= NP_001306978.1:p.Lys59=
NR_135131.1:n.319A=
NM_006331.8:c.176A= MANE Select NP_006322.4:p.Lys59=
NM_001320049.2:c.176A= NP_001306978.1:p.Lys59=
NR_135131.2:n.187A=