Canonical Allele Identifier: CA2014342581

Gene: EMG1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6974435C= , CM000674.2:g.6974435C=	GRCh38
NC_000012.11:g.7083597C= , CM000674.1:g.7083597C=	GRCh37
NC_000012.10:g.6953858C=	NCBI36
NG_021408.1:g.8655C=
NG_021408.2:g.8655C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000599672.6:c.265C= MANE Select	ENSP00000470560.1:p.His89=
ENST00000261406.7:c.247C=	ENSP00000476966.2:p.His83=
ENST00000539196.2:c.128C=
ENST00000599672.5:c.265C=	ENSP00000470560.1:p.His89=
ENST00000607161.5:c.268C=	ENSP00000480420.1:p.His90=
ENST00000611981.1:n.276C=
ENST00000620255.1:n.254C=
NM_006331.7:c.265C=	NP_006322.4:p.His89=
XM_011520907.1:c.265C=	XP_011519209.1:p.His89=
NM_001320049.1:c.265C=	NP_001306978.1:p.His89=
NR_135131.1:n.408C=
NM_006331.8:c.265C= MANE Select	NP_006322.4:p.His89=
NM_001320049.2:c.265C=	NP_001306978.1:p.His89=
NR_135131.2:n.276C=