Canonical Allele Identifier: CA2002974383

Gene: BACE1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.117289080G= , CM000673.2:g.117289080G=	GRCh38
NC_000011.9:g.117159796G= , CM000673.1:g.117159796G=	GRCh37
NC_000011.8:g.116665006G=	NCBI36
NG_029372.1:g.32177C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000313005.11:c.*486C= MANE Select	ENSP00000318585.6:n.*486C=
ENST00000679585.1:n.2435C=
ENST00000680271.1:n.1780C=
ENST00000680681.1:c.*718C=	ENSP00000505419.1:n.*718C=
ENST00000680800.1:n.1798C=
ENST00000680971.1:c.*486C=	ENSP00000506107.1:n.*486C=
ENST00000681714.1:n.1253C=
ENST00000681753.1:n.1195C=
ENST00000313005.10:c.*486C=	ENSP00000318585.6:n.*486C=
ENST00000392937.10:c.*486C=	ENSP00000475405.1:n.*486C=
ENST00000528053.5:c.*486C=	ENSP00000431848.1:n.*486C=
NM_001207048.1:c.*486C=	NP_001193977.1:n.*486C=
NM_001207049.1:c.*486C=	NP_001193978.1:n.*486C=
NM_012104.4:c.*486C=	NP_036236.1:n.*486C=
NM_138971.3:c.*486C=	NP_620427.1:n.*486C=
NM_138972.3:c.*486C=	NP_620428.1:n.*486C=
NM_138973.3:c.*486C=	NP_620429.1:n.*486C=
NM_001207048.2:c.*486C=	NP_001193977.1:n.*486C=
NM_001207049.2:c.*486C=	NP_001193978.1:n.*486C=
NM_001207048.3:c.*486C=	NP_001193977.1:n.*486C=
NM_001207049.3:c.*486C=	NP_001193978.1:n.*486C=
NM_012104.6:c.*486C= MANE Select	NP_036236.1:n.*486C=
NM_138971.4:c.*486C=	NP_620427.1:n.*486C=
NM_138972.4:c.*486C=	NP_620428.1:n.*486C=
NM_138973.4:c.*486C=	NP_620429.1:n.*486C=