Canonical Allele Identifier: CA1259891238

Gene: MCEE

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71124234G= , CM000664.2:g.71124234G=	GRCh38
NC_000002.11:g.71351364G= , CM000664.1:g.71351364G=	GRCh37
NC_000002.10:g.71204872G=	NCBI36
NG_008977.1:g.11031C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244217.6:c.350C= MANE Select	ENSP00000244217.5:p.Ala117=
ENST00000244217.5:c.350C=	ENSP00000244217.5:p.Ala117=
ENST00000413592.5:c.84+134C=	ENSP00000391140.1:n.84+134C=
ENST00000486135.1:c.65C=	ENSP00000441569.1:p.Ala22=
ENST00000494660.6:c.65C=	ENSP00000437361.1:p.Ala22=
NM_032601.3:c.350C=	NP_115990.3:p.Ala117=
XM_005264613.2:c.216+134C=	XP_005264670.1:n.216+134C=
XR_939729.1:n.419C=
XR_939729.2:n.419C=
NM_032601.4:c.350C= MANE Select	NP_115990.3:p.Ala117=