Canonical Allele Identifier: CA1259891232

Gene: MCEE

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71124217T= , CM000664.2:g.71124217T=	GRCh38
NC_000002.11:g.71351347T= , CM000664.1:g.71351347T=	GRCh37
NC_000002.10:g.71204855T=	NCBI36
NG_008977.1:g.11048A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244217.6:c.367A= MANE Select	ENSP00000244217.5:p.Ile123=
ENST00000244217.5:c.367A=	ENSP00000244217.5:p.Ile123=
ENST00000413592.5:c.84+151A=	ENSP00000391140.1:n.84+151A=
ENST00000486135.1:c.82A=	ENSP00000441569.1:p.Ile28=
ENST00000494660.6:c.82A=	ENSP00000437361.1:p.Ile28=
NM_032601.3:c.367A=	NP_115990.3:p.Ile123=
XM_005264613.2:c.216+151A=	XP_005264670.1:n.216+151A=
XR_939729.1:n.436A=
XR_939729.2:n.436A=
NM_032601.4:c.367A= MANE Select	NP_115990.3:p.Ile123=