Canonical Allele Identifier: CA2014342577

Gene: EMG1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6974428T= , CM000674.2:g.6974428T=	GRCh38
NC_000012.11:g.7083590T= , CM000674.1:g.7083590T=	GRCh37
NC_000012.10:g.6953851T=	NCBI36
NG_021408.1:g.8648T=
NG_021408.2:g.8648T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000599672.6:c.258T= MANE Select	ENSP00000470560.1:p.Asp86=
ENST00000261406.7:c.240T=	ENSP00000476966.2:p.Asp80=
ENST00000539196.2:c.121T=
ENST00000599672.5:c.258T=	ENSP00000470560.1:p.Asp86=
ENST00000607161.5:c.261T=	ENSP00000480420.1:p.Asp87=
ENST00000611981.1:n.269T=
ENST00000620255.1:n.247T=
NM_006331.7:c.258T=	NP_006322.4:p.Asp86=
XM_011520907.1:c.258T=	XP_011519209.1:p.Asp86=
NM_001320049.1:c.258T=	NP_001306978.1:p.Asp86=
NR_135131.1:n.401T=
NM_006331.8:c.258T= MANE Select	NP_006322.4:p.Asp86=
NM_001320049.2:c.258T=	NP_001306978.1:p.Asp86=
NR_135131.2:n.269T=