Canonical Allele Identifier: CA1259891106

Gene: MCEE

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71123928_71123929delinsTC , CM000664.2:g.71123928_71123929delinsTC	GRCh38
NC_000002.11:g.71351058_71351059delinsTC , CM000664.1:g.71351058_71351059delinsTC	GRCh37
NC_000002.10:g.71204566_71204567delinsTC	NCBI36
NG_008977.1:g.11336_11337delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244217.6:c.378+277_378+278delinsGA MANE Select	ENSP00000244217.5:n.378+277_378+278delinsGA
ENST00000244217.5:c.378+277_378+278delinsGA	ENSP00000244217.5:n.378+277_378+278delinsGA
ENST00000413592.5:c.84+439_84+440delinsGA	ENSP00000391140.1:n.84+439_84+440delinsGA
NM_032601.3:c.378+277_378+278delinsGA	NP_115990.3:n.378+277_378+278delinsGA
XM_005264613.2:c.216+439_216+440delinsGA	XP_005264670.1:n.216+439_216+440delinsGA
XR_939729.1:n.447+277_447+278delinsGA
XR_939729.2:n.447+277_447+278delinsGA
NM_032601.4:c.378+277_378+278delinsGA MANE Select	NP_115990.3:n.378+277_378+278delinsGA