Canonical Allele Identifier: CA2014342580

Gene: EMG1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6974434C= , CM000674.2:g.6974434C=	GRCh38
NC_000012.11:g.7083596C= , CM000674.1:g.7083596C=	GRCh37
NC_000012.10:g.6953857C=	NCBI36
NG_021408.1:g.8654C=
NG_021408.2:g.8654C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000599672.6:c.264C= MANE Select	ENSP00000470560.1:p.Thr88=
ENST00000261406.7:c.246C=	ENSP00000476966.2:p.Thr82=
ENST00000539196.2:c.127C=
ENST00000599672.5:c.264C=	ENSP00000470560.1:p.Thr88=
ENST00000607161.5:c.267C=	ENSP00000480420.1:p.Thr89=
ENST00000611981.1:n.275C=
ENST00000620255.1:n.253C=
NM_006331.7:c.264C=	NP_006322.4:p.Thr88=
XM_011520907.1:c.264C=	XP_011519209.1:p.Thr88=
NM_001320049.1:c.264C=	NP_001306978.1:p.Thr88=
NR_135131.1:n.407C=
NM_006331.8:c.264C= MANE Select	NP_006322.4:p.Thr88=
NM_001320049.2:c.264C=	NP_001306978.1:p.Thr88=
NR_135131.2:n.275C=