Canonical Allele Identifier: CA672260311
Gene: BACE1 HGNC NCBI

Linked Data

dbSNP Id: rs1371607887

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.117289090del , CM000673.2:g.117289090del GRCh38
NC_000011.9:g.117159806del , CM000673.1:g.117159806del GRCh37
NC_000011.8:g.116665016del NCBI36
NG_029372.1:g.32167del

Transcript Alleles

HGVS Amino-acid change
ENST00000313005.11:c.*476del MANE Select ENSP00000318585.6:n.*476del
ENST00000679585.1:n.2425del
ENST00000680271.1:n.1770del
ENST00000680681.1:c.*708del ENSP00000505419.1:n.*708del
ENST00000680800.1:n.1788del
ENST00000680971.1:c.*476del ENSP00000506107.1:n.*476del
ENST00000681714.1:n.1243del
ENST00000681753.1:n.1185del
ENST00000313005.10:c.*476del ENSP00000318585.6:n.*476del
ENST00000392937.10:c.*476del ENSP00000475405.1:n.*476del
ENST00000528053.5:c.*476del ENSP00000431848.1:n.*476del
NM_001207048.1:c.*476del NP_001193977.1:n.*476del
NM_001207049.1:c.*476del NP_001193978.1:n.*476del
NM_012104.4:c.*476del NP_036236.1:n.*476del
NM_138971.3:c.*476del NP_620427.1:n.*476del
NM_138972.3:c.*476del NP_620428.1:n.*476del
NM_138973.3:c.*476del NP_620429.1:n.*476del
NM_001207048.2:c.*476del NP_001193977.1:n.*476del
NM_001207049.2:c.*476del NP_001193978.1:n.*476del
NM_001207048.3:c.*476del NP_001193977.1:n.*476del
NM_001207049.3:c.*476del NP_001193978.1:n.*476del
NM_012104.6:c.*476del MANE Select NP_036236.1:n.*476del
NM_138971.4:c.*476del NP_620427.1:n.*476del
NM_138972.4:c.*476del NP_620428.1:n.*476del
NM_138973.4:c.*476del NP_620429.1:n.*476del