Canonical Allele Identifier: CA15678118
Gene: BACE1 HGNC NCBI
RNF214 HGNC NCBI

Linked Data

dbSNP Id: rs1047964

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.117286177G>C , CM000673.2:g.117286177G>C GRCh38
NC_000011.9:g.117156893G>C , CM000673.1:g.117156893G>C GRCh37
NC_000011.8:g.116662103G>C NCBI36
NG_029372.1:g.35080C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000313005.11:c.*3389C>G (BACE1) MANE Select ENSP00000318585.6:n.*3389C>G
ENST00000300650.9:c.*1026G>C (RNF214) MANE Select ENSP00000300650.4:n.*1026G>C
ENST00000679585.1:n.5338C>G (BACE1)
ENST00000680271.1:n.4683C>G (BACE1)
ENST00000680800.1:n.4701C>G (BACE1)
ENST00000680971.1:c.*3389C>G (BACE1) ENSP00000506107.1:n.*3389C>G
ENST00000313005.10:c.*3389C>G (BACE1) ENSP00000318585.6:n.*3389C>G
ENST00000392937.10:c.*3389C>G (BACE1) ENSP00000475405.1:n.*3389C>G
ENST00000530849.1:c.*1026G>C (RNF214) ENSP00000432903.1:n.*1026G>C
NM_001207048.1:c.*3389C>G (BACE1) NP_001193977.1:n.*3389C>G
NM_001207049.1:c.*3389C>G (BACE1) NP_001193978.1:n.*3389C>G
NM_012104.4:c.*3389C>G (BACE1) NP_036236.1:n.*3389C>G
NM_138971.3:c.*3389C>G (BACE1) NP_620427.1:n.*3389C>G
NM_138972.3:c.*3389C>G (BACE1) NP_620428.1:n.*3389C>G
NM_138973.3:c.*3389C>G (BACE1) NP_620429.1:n.*3389C>G
NM_207343.4:c.*1026G>C (RNF214) MANE Select NP_997226.2:n.*1026G>C
NM_001207048.2:c.*3389C>G (BACE1) NP_001193977.1:n.*3389C>G
NM_001207049.2:c.*3389C>G (BACE1) NP_001193978.1:n.*3389C>G
NM_001077239.2:c.*1026G>C (RNF214) NP_001070707.1:n.*1026G>C
NM_001207048.3:c.*3389C>G (BACE1) NP_001193977.1:n.*3389C>G
NM_001207049.3:c.*3389C>G (BACE1) NP_001193978.1:n.*3389C>G
NM_001278249.2:c.*1026G>C (RNF214) NP_001265178.1:n.*1026G>C
NM_012104.6:c.*3389C>G (BACE1) MANE Select NP_036236.1:n.*3389C>G
NM_138971.4:c.*3389C>G (BACE1) NP_620427.1:n.*3389C>G
NM_138972.4:c.*3389C>G (BACE1) NP_620428.1:n.*3389C>G
NM_138973.4:c.*3389C>G (BACE1) NP_620429.1:n.*3389C>G