Canonical Allele Identifier: CA1259891164

Gene: MCEE

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71124065_71124068delinsTGAG , CM000664.2:g.71124065_71124068delinsTGAG	GRCh38
NC_000002.11:g.71351195_71351198delinsTGAG , CM000664.1:g.71351195_71351198delinsTGAG	GRCh37
NC_000002.10:g.71204703_71204706delinsTGAG	NCBI36
NG_008977.1:g.11197_11200delinsCTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244217.6:c.378+138_378+141delinsCTCA MANE Select	ENSP00000244217.5:n.378+138_378+141delinsCTCA
ENST00000244217.5:c.378+138_378+141delinsCTCA	ENSP00000244217.5:n.378+138_378+141delinsCTCA
ENST00000413592.5:c.84+300_84+303delinsCTCA	ENSP00000391140.1:n.84+300_84+303delinsCTCA
NM_032601.3:c.378+138_378+141delinsCTCA	NP_115990.3:n.378+138_378+141delinsCTCA
XM_005264613.2:c.216+300_216+303delinsCTCA	XP_005264670.1:n.216+300_216+303delinsCTCA
XR_939729.1:n.447+138_447+141delinsCTCA
XR_939729.2:n.447+138_447+141delinsCTCA
NM_032601.4:c.378+138_378+141delinsCTCA MANE Select	NP_115990.3:n.378+138_378+141delinsCTCA