Canonical Allele Identifier: CA2725065553
Gene: BACE1 HGNC NCBI

Linked Data

dbSNP Id: rs2134439198

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.117289083T>C , CM000673.2:g.117289083T>C GRCh38
NC_000011.9:g.117159799T>C , CM000673.1:g.117159799T>C GRCh37
NC_000011.8:g.116665009T>C NCBI36
NG_029372.1:g.32174A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000313005.11:c.*483A>G MANE Select ENSP00000318585.6:n.*483A>G
ENST00000679585.1:n.2432A>G
ENST00000680271.1:n.1777A>G
ENST00000680681.1:c.*715A>G ENSP00000505419.1:n.*715A>G
ENST00000680800.1:n.1795A>G
ENST00000680971.1:c.*483A>G ENSP00000506107.1:n.*483A>G
ENST00000681714.1:n.1250A>G
ENST00000681753.1:n.1192A>G
ENST00000313005.10:c.*483A>G ENSP00000318585.6:n.*483A>G
ENST00000392937.10:c.*483A>G ENSP00000475405.1:n.*483A>G
ENST00000528053.5:c.*483A>G ENSP00000431848.1:n.*483A>G
NM_001207048.1:c.*483A>G NP_001193977.1:n.*483A>G
NM_001207049.1:c.*483A>G NP_001193978.1:n.*483A>G
NM_012104.4:c.*483A>G NP_036236.1:n.*483A>G
NM_138971.3:c.*483A>G NP_620427.1:n.*483A>G
NM_138972.3:c.*483A>G NP_620428.1:n.*483A>G
NM_138973.3:c.*483A>G NP_620429.1:n.*483A>G
NM_001207048.2:c.*483A>G NP_001193977.1:n.*483A>G
NM_001207049.2:c.*483A>G NP_001193978.1:n.*483A>G
NM_001207048.3:c.*483A>G NP_001193977.1:n.*483A>G
NM_001207049.3:c.*483A>G NP_001193978.1:n.*483A>G
NM_012104.6:c.*483A>G MANE Select NP_036236.1:n.*483A>G
NM_138971.4:c.*483A>G NP_620427.1:n.*483A>G
NM_138972.4:c.*483A>G NP_620428.1:n.*483A>G
NM_138973.4:c.*483A>G NP_620429.1:n.*483A>G