Canonical Allele Identifier: CA1259891229

Gene: MCEE

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71124211T= , CM000664.2:g.71124211T=	GRCh38
NC_000002.11:g.71351341T= , CM000664.1:g.71351341T=	GRCh37
NC_000002.10:g.71204849T=	NCBI36
NG_008977.1:g.11054A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244217.6:c.373A= MANE Select	ENSP00000244217.5:p.Ile125=
ENST00000244217.5:c.373A=	ENSP00000244217.5:p.Ile125=
ENST00000413592.5:c.84+157A=	ENSP00000391140.1:n.84+157A=
ENST00000486135.1:c.88A=	ENSP00000441569.1:p.Ile30=
ENST00000494660.6:c.88A=	ENSP00000437361.1:p.Ile30=
NM_032601.3:c.373A=	NP_115990.3:p.Ile125=
XM_005264613.2:c.216+157A=	XP_005264670.1:n.216+157A=
XR_939729.1:n.442A=
XR_939729.2:n.442A=
NM_032601.4:c.373A= MANE Select	NP_115990.3:p.Ile125=