Canonical Allele Identifier: CA426689614

Gene: MCEE

Linked Data

• MyVariant Identifiers: chr2:g.71351384A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71124254A>C , CM000664.2:g.71124254A>C	GRCh38
NC_000002.11:g.71351384A>C , CM000664.1:g.71351384A>C	GRCh37
NC_000002.10:g.71204892A>C	NCBI36
NG_008977.1:g.11011T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244217.6:c.330T>G MANE Select	ENSP00000244217.5:p.Gly110=
ENST00000244217.5:c.330T>G	ENSP00000244217.5:p.Gly110=
ENST00000413592.5:c.84+114T>G	ENSP00000391140.1:n.84+114T>G
ENST00000486135.1:c.45T>G	ENSP00000441569.1:p.Gly15=
ENST00000494660.6:c.45T>G	ENSP00000437361.1:p.Gly15=
NM_032601.3:c.330T>G	NP_115990.3:p.Gly110=
XM_005264613.2:c.216+114T>G	XP_005264670.1:n.216+114T>G
XR_939729.1:n.399T>G
XR_939729.2:n.399T>G
NM_032601.4:c.330T>G MANE Select	NP_115990.3:p.Gly110=