Canonical Allele Identifier: CA426692002

Gene: MCEE

Linked Data

• MyVariant Identifiers: chr2:g.71351642T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71124512T>A , CM000664.2:g.71124512T>A	GRCh38
NC_000002.11:g.71351642T>A , CM000664.1:g.71351642T>A	GRCh37
NC_000002.10:g.71205150T>A	NCBI36
NG_008977.1:g.10753A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244217.6:c.72A>T MANE Select	ENSP00000244217.5:p.Pro24=
ENST00000244217.5:c.72A>T	ENSP00000244217.5:p.Pro24=
ENST00000486135.1:c.-214A>T	ENSP00000441569.1:n.-214A>T
ENST00000494660.6:c.-214A>T	ENSP00000437361.1:n.-214A>T
NM_032601.3:c.72A>T	NP_115990.3:p.Pro24=
XM_005264613.2:c.72A>T	XP_005264670.1:p.Pro24=
XR_939729.1:n.141A>T
XR_939729.2:n.141A>T
NM_032601.4:c.72A>T MANE Select	NP_115990.3:p.Pro24=