Canonical Allele Identifier: CA2014342579

Gene: EMG1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6974432A= , CM000674.2:g.6974432A=	GRCh38
NC_000012.11:g.7083594A= , CM000674.1:g.7083594A=	GRCh37
NC_000012.10:g.6953855A=	NCBI36
NG_021408.1:g.8652A=
NG_021408.2:g.8652A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000599672.6:c.262A= MANE Select	ENSP00000470560.1:p.Thr88=
ENST00000261406.7:c.244A=	ENSP00000476966.2:p.Thr82=
ENST00000539196.2:c.125A=
ENST00000599672.5:c.262A=	ENSP00000470560.1:p.Thr88=
ENST00000607161.5:c.265A=	ENSP00000480420.1:p.Thr89=
ENST00000611981.1:n.273A=
ENST00000620255.1:n.251A=
NM_006331.7:c.262A=	NP_006322.4:p.Thr88=
XM_011520907.1:c.262A=	XP_011519209.1:p.Thr88=
NM_001320049.1:c.262A=	NP_001306978.1:p.Thr88=
NR_135131.1:n.405A=
NM_006331.8:c.262A= MANE Select	NP_006322.4:p.Thr88=
NM_001320049.2:c.262A=	NP_001306978.1:p.Thr88=
NR_135131.2:n.273A=