Canonical Allele Identifier: CA1259891289

Gene: MCEE

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71124357_71124358delinsGC , CM000664.2:g.71124357_71124358delinsGC	GRCh38
NC_000002.11:g.71351487_71351488delinsGC , CM000664.1:g.71351487_71351488delinsGC	GRCh37
NC_000002.10:g.71204995_71204996delinsGC	NCBI36
NG_008977.1:g.10907_10908delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244217.6:c.226_227delinsGC MANE Select	ENSP00000244217.5:p.Ala76=
ENST00000244217.5:c.226_227delinsGC	ENSP00000244217.5:p.Ala76=
ENST00000413592.5:c.84+10_84+11delinsGC	ENSP00000391140.1:n.84+10_84+11delinsGC
ENST00000486135.1:c.-60_-59delinsGC	ENSP00000441569.1:n.-60_-59delinsGC
ENST00000494660.6:c.-60_-59delinsGC	ENSP00000437361.1:n.-60_-59delinsGC
NM_032601.3:c.226_227delinsGC	NP_115990.3:p.Ala76=
XM_005264613.2:c.216+10_216+11delinsGC	XP_005264670.1:n.216+10_216+11delinsGC
XR_939729.1:n.295_296delinsGC
XR_939729.2:n.295_296delinsGC
NM_032601.4:c.226_227delinsGC MANE Select	NP_115990.3:p.Ala76=