Canonical Allele Identifier: CA1259891306

Gene: MCEE

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71124408T= , CM000664.2:g.71124408T=	GRCh38
NC_000002.11:g.71351538T= , CM000664.1:g.71351538T=	GRCh37
NC_000002.10:g.71205046T=	NCBI36
NG_008977.1:g.10857A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244217.6:c.176A= MANE Select	ENSP00000244217.5:p.Glu59=
ENST00000244217.5:c.176A=	ENSP00000244217.5:p.Glu59=
ENST00000413592.5:c.44A=	ENSP00000391140.1:p.Glu15=
ENST00000486135.1:c.-110A=	ENSP00000441569.1:n.-110A=
ENST00000494660.6:c.-110A=	ENSP00000437361.1:n.-110A=
NM_032601.3:c.176A=	NP_115990.3:p.Glu59=
XM_005264613.2:c.176A=	XP_005264670.1:p.Glu59=
XR_939729.1:n.245A=
XR_939729.2:n.245A=
NM_032601.4:c.176A= MANE Select	NP_115990.3:p.Glu59=