Canonical Allele Identifier: CA2014342611

Gene: EMG1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6974489G= , CM000674.2:g.6974489G=	GRCh38
NC_000012.11:g.7083651G= , CM000674.1:g.7083651G=	GRCh37
NC_000012.10:g.6953912G=	NCBI36
NG_021408.1:g.8709G=
NG_021408.2:g.8709G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599672.6:c.270+49G= MANE Select	ENSP00000470560.1:n.270+49G=
ENST00000261406.7:c.252+49G=	ENSP00000476966.2:n.252+49G=
ENST00000539196.2:c.133+49G=
ENST00000599672.5:c.270+49G=	ENSP00000470560.1:n.270+49G=
ENST00000607161.5:c.273+49G=	ENSP00000480420.1:n.273+49G=
ENST00000611981.1:n.281+49G=
ENST00000620255.1:n.308G=
NM_006331.7:c.270+49G=	NP_006322.4:n.270+49G=
XM_011520907.1:c.270+49G=	XP_011519209.1:n.270+49G=
NM_001320049.1:c.270+49G=	NP_001306978.1:n.270+49G=
NR_135131.1:n.413+49G=
NM_006331.8:c.270+49G= MANE Select	NP_006322.4:n.270+49G=
NM_001320049.2:c.270+49G=	NP_001306978.1:n.270+49G=
NR_135131.2:n.281+49G=