Canonical Allele Identifier: CA2014342582

Gene: EMG1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6974438C= , CM000674.2:g.6974438C=	GRCh38
NC_000012.11:g.7083600C= , CM000674.1:g.7083600C=	GRCh37
NC_000012.10:g.6953861C=	NCBI36
NG_021408.1:g.8658C=
NG_021408.2:g.8658C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000599672.6:c.268C= MANE Select	ENSP00000470560.1:p.Gln90=
ENST00000261406.7:c.250C=	ENSP00000476966.2:p.Gln84=
ENST00000539196.2:c.131C=
ENST00000599672.5:c.268C=	ENSP00000470560.1:p.Gln90=
ENST00000607161.5:c.271C=	ENSP00000480420.1:p.Gln91=
ENST00000611981.1:n.279C=
ENST00000620255.1:n.257C=
NM_006331.7:c.268C=	NP_006322.4:p.Gln90=
XM_011520907.1:c.268C=	XP_011519209.1:p.Gln90=
NM_001320049.1:c.268C=	NP_001306978.1:p.Gln90=
NR_135131.1:n.411C=
NM_006331.8:c.268C= MANE Select	NP_006322.4:p.Gln90=
NM_001320049.2:c.268C=	NP_001306978.1:p.Gln90=
NR_135131.2:n.279C=