Canonical Allele Identifier: CA347189516

Gene: MCEE

Linked Data

• MyVariant Identifiers: chr2:g.71351605G>T (hg19) ; chr2:g.71124475G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71124475G>T , CM000664.2:g.71124475G>T	GRCh38
NC_000002.11:g.71351605G>T , CM000664.1:g.71351605G>T	GRCh37
NC_000002.10:g.71205113G>T	NCBI36
NG_008977.1:g.10790C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244217.6:c.109C>A MANE Select	ENSP00000244217.5:p.Gln37Lys
ENST00000244217.5:c.109C>A	ENSP00000244217.5:p.Gln37Lys
ENST00000486135.1:c.-177C>A	ENSP00000441569.1:n.-177C>A
ENST00000494660.6:c.-177C>A	ENSP00000437361.1:n.-177C>A
NM_032601.3:c.109C>A	NP_115990.3:p.Gln37Lys
XM_005264613.2:c.109C>A	XP_005264670.1:p.Gln37Lys
XR_939729.1:n.178C>A
XR_939729.2:n.178C>A
NM_032601.4:c.109C>A MANE Select	NP_115990.3:p.Gln37Lys