Canonical Allele Identifier: CA1259891233

Gene: MCEE

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71124222T= , CM000664.2:g.71124222T=	GRCh38
NC_000002.11:g.71351352T= , CM000664.1:g.71351352T=	GRCh37
NC_000002.10:g.71204860T=	NCBI36
NG_008977.1:g.11043A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244217.6:c.362A= MANE Select	ENSP00000244217.5:p.His121=
ENST00000244217.5:c.362A=	ENSP00000244217.5:p.His121=
ENST00000413592.5:c.84+146A=	ENSP00000391140.1:n.84+146A=
ENST00000486135.1:c.77A=	ENSP00000441569.1:p.His26=
ENST00000494660.6:c.77A=	ENSP00000437361.1:p.His26=
NM_032601.3:c.362A=	NP_115990.3:p.His121=
XM_005264613.2:c.216+146A=	XP_005264670.1:n.216+146A=
XR_939729.1:n.431A=
XR_939729.2:n.431A=
NM_032601.4:c.362A= MANE Select	NP_115990.3:p.His121=