Canonical Allele Identifier: CA2616166819
Gene: BACE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.117288993_117288994insA , CM000673.2:g.117288993_117288994insA GRCh38
NC_000011.9:g.117159709_117159710insA , CM000673.1:g.117159709_117159710insA GRCh37
NC_000011.8:g.116664919_116664920insA NCBI36
NG_029372.1:g.32263_32264insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000313005.11:c.*572_*573insT MANE Select ENSP00000318585.6:n.*572_*573insT
ENST00000679585.1:n.2521_2522insT
ENST00000680271.1:n.1866_1867insT
ENST00000680681.1:c.*804_*805insT ENSP00000505419.1:n.*804_*805insT
ENST00000680800.1:n.1884_1885insT
ENST00000680971.1:c.*572_*573insT ENSP00000506107.1:n.*572_*573insT
ENST00000313005.10:c.*572_*573insT ENSP00000318585.6:n.*572_*573insT
ENST00000392937.10:c.*572_*573insT ENSP00000475405.1:n.*572_*573insT
ENST00000528053.5:c.*572_*573insT ENSP00000431848.1:n.*572_*573insT
NM_001207048.1:c.*572_*573insT NP_001193977.1:n.*572_*573insT
NM_001207049.1:c.*572_*573insT NP_001193978.1:n.*572_*573insT
NM_012104.4:c.*572_*573insT NP_036236.1:n.*572_*573insT
NM_138971.3:c.*572_*573insT NP_620427.1:n.*572_*573insT
NM_138972.3:c.*572_*573insT NP_620428.1:n.*572_*573insT
NM_138973.3:c.*572_*573insT NP_620429.1:n.*572_*573insT
NM_001207048.2:c.*572_*573insT NP_001193977.1:n.*572_*573insT
NM_001207049.2:c.*572_*573insT NP_001193978.1:n.*572_*573insT
NM_001207048.3:c.*572_*573insT NP_001193977.1:n.*572_*573insT
NM_001207049.3:c.*572_*573insT NP_001193978.1:n.*572_*573insT
NM_012104.6:c.*572_*573insT MANE Select NP_036236.1:n.*572_*573insT
NM_138971.4:c.*572_*573insT NP_620427.1:n.*572_*573insT
NM_138972.4:c.*572_*573insT NP_620428.1:n.*572_*573insT
NM_138973.4:c.*572_*573insT NP_620429.1:n.*572_*573insT