Canonical Allele Identifier: CA645529097

Gene: MCEE

Linked Data

• COSMIC: COSM301422

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71124377_71124378delinsAG , CM000664.2:g.71124377_71124378delinsAG	GRCh38
NC_000002.11:g.71351507_71351508delinsAG , CM000664.1:g.71351507_71351508delinsAG	GRCh37
NC_000002.10:g.71205015_71205016delinsAG	NCBI36
NG_008977.1:g.10887_10888delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244217.6:c.206_207delinsCT MANE Select	ENSP00000244217.5:p.Leu69Pro
ENST00000244217.5:c.206_207delinsCT	ENSP00000244217.5:p.Leu69Pro
ENST00000413592.5:c.74_75delinsCT	ENSP00000391140.1:p.Leu25Pro
ENST00000486135.1:c.-80_-79delinsCT	ENSP00000441569.1:n.-80_-79delinsCT
ENST00000494660.6:c.-80_-79delinsCT	ENSP00000437361.1:n.-80_-79delinsCT
NM_032601.3:c.206_207delinsCT	NP_115990.3:p.Leu69Pro
XM_005264613.2:c.206_207delinsCT	XP_005264670.1:p.Leu69Pro
XR_939729.1:n.275_276delinsCT
XR_939729.2:n.275_276delinsCT
NM_032601.4:c.206_207delinsCT MANE Select	NP_115990.3:p.Leu69Pro