Canonical Allele Identifier: CA426690975

Gene: MCEE

Linked Data

• MyVariant Identifiers: chr2:g.71351525T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71124395T>A , CM000664.2:g.71124395T>A	GRCh38
NC_000002.11:g.71351525T>A , CM000664.1:g.71351525T>A	GRCh37
NC_000002.10:g.71205033T>A	NCBI36
NG_008977.1:g.10870A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244217.6:c.189A>T MANE Select	ENSP00000244217.5:p.Ala63=
ENST00000244217.5:c.189A>T	ENSP00000244217.5:p.Ala63=
ENST00000413592.5:c.57A>T	ENSP00000391140.1:p.Ala19=
ENST00000486135.1:c.-97A>T	ENSP00000441569.1:n.-97A>T
ENST00000494660.6:c.-97A>T	ENSP00000437361.1:n.-97A>T
NM_032601.3:c.189A>T	NP_115990.3:p.Ala63=
XM_005264613.2:c.189A>T	XP_005264670.1:p.Ala63=
XR_939729.1:n.258A>T
XR_939729.2:n.258A>T
NM_032601.4:c.189A>T MANE Select	NP_115990.3:p.Ala63=