Canonical Allele Identifier: CA1259891107

Gene: MCEE

Linked Data

• dbSNP Id: rs1673155337

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71123929del , CM000664.2:g.71123929del	GRCh38
NC_000002.11:g.71351059del , CM000664.1:g.71351059del	GRCh37
NC_000002.10:g.71204567del	NCBI36
NG_008977.1:g.11336del

Transcript Alleles

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