Canonical Allele Identifier: CA1259891328

Gene: MCEE

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71124453T= , CM000664.2:g.71124453T=	GRCh38
NC_000002.11:g.71351583T= , CM000664.1:g.71351583T=	GRCh37
NC_000002.10:g.71205091T=	NCBI36
NG_008977.1:g.10812A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000244217.6:c.131A= MANE Select	ENSP00000244217.5:p.Asn44=
ENST00000244217.5:c.131A=	ENSP00000244217.5:p.Asn44=
ENST00000486135.1:c.-155A=	ENSP00000441569.1:n.-155A=
ENST00000494660.6:c.-155A=	ENSP00000437361.1:n.-155A=
NM_032601.3:c.131A=	NP_115990.3:p.Asn44=
XM_005264613.2:c.131A=	XP_005264670.1:p.Asn44=
XR_939729.1:n.200A=
XR_939729.2:n.200A=
NM_032601.4:c.131A= MANE Select	NP_115990.3:p.Asn44=