Canonical Allele Identifier: CA2002974392
Gene: BACE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.117289112C= , CM000673.2:g.117289112C= GRCh38
NC_000011.9:g.117159828C= , CM000673.1:g.117159828C= GRCh37
NC_000011.8:g.116665038C= NCBI36
NG_029372.1:g.32145G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000313005.11:c.*454G= MANE Select ENSP00000318585.6:n.*454G=
ENST00000679585.1:n.2403G=
ENST00000680271.1:n.1748G=
ENST00000680681.1:c.*686G= ENSP00000505419.1:n.*686G=
ENST00000680800.1:n.1766G=
ENST00000680971.1:c.*454G= ENSP00000506107.1:n.*454G=
ENST00000681714.1:n.1221G=
ENST00000681753.1:n.1163G=
ENST00000313005.10:c.*454G= ENSP00000318585.6:n.*454G=
ENST00000392937.10:c.*454G= ENSP00000475405.1:n.*454G=
ENST00000528053.5:c.*454G= ENSP00000431848.1:n.*454G=
NM_001207048.1:c.*454G= NP_001193977.1:n.*454G=
NM_001207049.1:c.*454G= NP_001193978.1:n.*454G=
NM_012104.4:c.*454G= NP_036236.1:n.*454G=
NM_138971.3:c.*454G= NP_620427.1:n.*454G=
NM_138972.3:c.*454G= NP_620428.1:n.*454G=
NM_138973.3:c.*454G= NP_620429.1:n.*454G=
NM_001207048.2:c.*454G= NP_001193977.1:n.*454G=
NM_001207049.2:c.*454G= NP_001193978.1:n.*454G=
NM_001207048.3:c.*454G= NP_001193977.1:n.*454G=
NM_001207049.3:c.*454G= NP_001193978.1:n.*454G=
NM_012104.6:c.*454G= MANE Select NP_036236.1:n.*454G=
NM_138971.4:c.*454G= NP_620427.1:n.*454G=
NM_138972.4:c.*454G= NP_620428.1:n.*454G=
NM_138973.4:c.*454G= NP_620429.1:n.*454G=