Canonical Allele Identifier: CA1259891249

Gene: MCEE

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71124273C= , CM000664.2:g.71124273C=	GRCh38
NC_000002.11:g.71351403C= , CM000664.1:g.71351403C=	GRCh37
NC_000002.10:g.71204911C=	NCBI36
NG_008977.1:g.10992G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244217.6:c.311G= MANE Select	ENSP00000244217.5:p.Arg104=
ENST00000244217.5:c.311G=	ENSP00000244217.5:p.Arg104=
ENST00000413592.5:c.84+95G=	ENSP00000391140.1:n.84+95G=
ENST00000486135.1:c.26G=	ENSP00000441569.1:p.Arg9=
ENST00000494660.6:c.26G=	ENSP00000437361.1:p.Arg9=
NM_032601.3:c.311G=	NP_115990.3:p.Arg104=
XM_005264613.2:c.216+95G=	XP_005264670.1:n.216+95G=
XR_939729.1:n.380G=
XR_939729.2:n.380G=
NM_032601.4:c.311G= MANE Select	NP_115990.3:p.Arg104=