Canonical Allele Identifier: CA2659522911

Gene: MCEE

Linked Data

• gnomAD v4: 2-71124573-TCTTTTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71124574_71124579del , CM000664.2:g.71124574_71124579del	GRCh38
NC_000002.11:g.71351704_71351709del , CM000664.1:g.71351704_71351709del	GRCh37
NC_000002.10:g.71205212_71205217del	NCBI36
NG_008977.1:g.10686_10691del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244217.6:c.41-36_41-31del MANE Select	ENSP00000244217.5:n.41-36_41-31del
ENST00000244217.5:c.41-36_41-31del	ENSP00000244217.5:n.41-36_41-31del
ENST00000486135.1:c.-245-36_-245-31del	ENSP00000441569.1:n.-245-36_-245-31del
ENST00000494660.6:c.-245-36_-245-31del	ENSP00000437361.1:n.-245-36_-245-31del
NM_032601.3:c.41-36_41-31del	NP_115990.3:n.41-36_41-31del
XM_005264613.2:c.41-36_41-31del	XP_005264670.1:n.41-36_41-31del
XR_939729.1:n.110-36_110-31del
XR_939729.2:n.110-36_110-31del
NM_032601.4:c.41-36_41-31del MANE Select	NP_115990.3:n.41-36_41-31del