Canonical Allele Identifier: CA1259891302

Gene: MCEE

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71124402G= , CM000664.2:g.71124402G=	GRCh38
NC_000002.11:g.71351532G= , CM000664.1:g.71351532G=	GRCh37
NC_000002.10:g.71205040G=	NCBI36
NG_008977.1:g.10863C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244217.6:c.182C= MANE Select	ENSP00000244217.5:p.Ala61=
ENST00000244217.5:c.182C=	ENSP00000244217.5:p.Ala61=
ENST00000413592.5:c.50C=	ENSP00000391140.1:p.Ala17=
ENST00000486135.1:c.-104C=	ENSP00000441569.1:n.-104C=
ENST00000494660.6:c.-104C=	ENSP00000437361.1:n.-104C=
NM_032601.3:c.182C=	NP_115990.3:p.Ala61=
XM_005264613.2:c.182C=	XP_005264670.1:p.Ala61=
XR_939729.1:n.251C=
XR_939729.2:n.251C=
NM_032601.4:c.182C= MANE Select	NP_115990.3:p.Ala61=