Canonical Allele Identifier: CA1259891329

Gene: MCEE

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71124455C= , CM000664.2:g.71124455C=	GRCh38
NC_000002.11:g.71351585C= , CM000664.1:g.71351585C=	GRCh37
NC_000002.10:g.71205093C=	NCBI36
NG_008977.1:g.10810G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244217.6:c.129G= MANE Select	ENSP00000244217.5:p.Trp43=
ENST00000244217.5:c.129G=	ENSP00000244217.5:p.Trp43=
ENST00000486135.1:c.-157G=	ENSP00000441569.1:n.-157G=
ENST00000494660.6:c.-157G=	ENSP00000437361.1:n.-157G=
NM_032601.3:c.129G=	NP_115990.3:p.Trp43=
XM_005264613.2:c.129G=	XP_005264670.1:p.Trp43=
XR_939729.1:n.198G=
XR_939729.2:n.198G=
NM_032601.4:c.129G= MANE Select	NP_115990.3:p.Trp43=