Canonical Allele Identifier: CA2014342540
Gene: EMG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6974352A= , CM000674.2:g.6974352A= GRCh38
NC_000012.11:g.7083514A= , CM000674.1:g.7083514A= GRCh37
NC_000012.10:g.6953775A= NCBI36
NG_021408.1:g.8572A=
NG_021408.2:g.8572A=

Transcript Alleles

HGVS Amino-acid change
ENST00000599672.6:c.182A= MANE Select ENSP00000470560.1:p.Tyr61=
ENST00000261406.7:c.164A= ENSP00000476966.2:p.Tyr55=
ENST00000539196.2:c.45A=
ENST00000599672.5:c.182A= ENSP00000470560.1:p.Tyr61=
ENST00000607161.5:c.185A= ENSP00000480420.1:p.Tyr62=
ENST00000611981.1:n.193A=
ENST00000620255.1:n.171A=
NM_006331.7:c.182A= NP_006322.4:p.Tyr61=
XM_011520907.1:c.182A= XP_011519209.1:p.Tyr61=
NM_001320049.1:c.182A= NP_001306978.1:p.Tyr61=
NR_135131.1:n.325A=
NM_006331.8:c.182A= MANE Select NP_006322.4:p.Tyr61=
NM_001320049.2:c.182A= NP_001306978.1:p.Tyr61=
NR_135131.2:n.193A=