Canonical Allele Identifier: CA1259891299

Gene: MCEE

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71124392A= , CM000664.2:g.71124392A=	GRCh38
NC_000002.11:g.71351522A= , CM000664.1:g.71351522A=	GRCh37
NC_000002.10:g.71205030A=	NCBI36
NG_008977.1:g.10873T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244217.6:c.192T= MANE Select	ENSP00000244217.5:p.Phe64=
ENST00000244217.5:c.192T=	ENSP00000244217.5:p.Phe64=
ENST00000413592.5:c.60T=	ENSP00000391140.1:p.Phe20=
ENST00000486135.1:c.-94T=	ENSP00000441569.1:n.-94T=
ENST00000494660.6:c.-94T=	ENSP00000437361.1:n.-94T=
NM_032601.3:c.192T=	NP_115990.3:p.Phe64=
XM_005264613.2:c.192T=	XP_005264670.1:p.Phe64=
XR_939729.1:n.261T=
XR_939729.2:n.261T=
NM_032601.4:c.192T= MANE Select	NP_115990.3:p.Phe64=