Canonical Allele Identifier: CA2616166914

Gene: BACE1

Linked Data

• gnomAD v4: 11-117289105-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.117289105G>A , CM000673.2:g.117289105G>A	GRCh38
NC_000011.9:g.117159821G>A , CM000673.1:g.117159821G>A	GRCh37
NC_000011.8:g.116665031G>A	NCBI36
NG_029372.1:g.32152C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313005.11:c.*461C>T MANE Select	ENSP00000318585.6:n.*461C>T
ENST00000679585.1:n.2410C>T
ENST00000680271.1:n.1755C>T
ENST00000680681.1:c.*693C>T	ENSP00000505419.1:n.*693C>T
ENST00000680800.1:n.1773C>T
ENST00000680971.1:c.*461C>T	ENSP00000506107.1:n.*461C>T
ENST00000681714.1:n.1228C>T
ENST00000681753.1:n.1170C>T
ENST00000313005.10:c.*461C>T	ENSP00000318585.6:n.*461C>T
ENST00000392937.10:c.*461C>T	ENSP00000475405.1:n.*461C>T
ENST00000528053.5:c.*461C>T	ENSP00000431848.1:n.*461C>T
NM_001207048.1:c.*461C>T	NP_001193977.1:n.*461C>T
NM_001207049.1:c.*461C>T	NP_001193978.1:n.*461C>T
NM_012104.4:c.*461C>T	NP_036236.1:n.*461C>T
NM_138971.3:c.*461C>T	NP_620427.1:n.*461C>T
NM_138972.3:c.*461C>T	NP_620428.1:n.*461C>T
NM_138973.3:c.*461C>T	NP_620429.1:n.*461C>T
NM_001207048.2:c.*461C>T	NP_001193977.1:n.*461C>T
NM_001207049.2:c.*461C>T	NP_001193978.1:n.*461C>T
NM_001207048.3:c.*461C>T	NP_001193977.1:n.*461C>T
NM_001207049.3:c.*461C>T	NP_001193978.1:n.*461C>T
NM_012104.6:c.*461C>T MANE Select	NP_036236.1:n.*461C>T
NM_138971.4:c.*461C>T	NP_620427.1:n.*461C>T
NM_138972.4:c.*461C>T	NP_620428.1:n.*461C>T
NM_138973.4:c.*461C>T	NP_620429.1:n.*461C>T