Canonical Allele Identifier: CA426689590

Gene: MCEE

Linked Data

• MyVariant Identifiers: chr2:g.71351381A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71124251A>G , CM000664.2:g.71124251A>G	GRCh38
NC_000002.11:g.71351381A>G , CM000664.1:g.71351381A>G	GRCh37
NC_000002.10:g.71204889A>G	NCBI36
NG_008977.1:g.11014T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244217.6:c.333T>C MANE Select	ENSP00000244217.5:p.Phe111=
ENST00000244217.5:c.333T>C	ENSP00000244217.5:p.Phe111=
ENST00000413592.5:c.84+117T>C	ENSP00000391140.1:n.84+117T>C
ENST00000486135.1:c.48T>C	ENSP00000441569.1:p.Phe16=
ENST00000494660.6:c.48T>C	ENSP00000437361.1:p.Phe16=
NM_032601.3:c.333T>C	NP_115990.3:p.Phe111=
XM_005264613.2:c.216+117T>C	XP_005264670.1:n.216+117T>C
XR_939729.1:n.402T>C
XR_939729.2:n.402T>C
NM_032601.4:c.333T>C MANE Select	NP_115990.3:p.Phe111=