Canonical Allele Identifier: CA2654122660

Gene: APP

Linked Data

• gnomAD v4: 21-25881361-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25881361T>C , CM000683.2:g.25881361T>C	GRCh38
NC_000021.8:g.27253672T>C , CM000683.1:g.27253672T>C	GRCh37
NC_000021.7:g.26175543T>C	NCBI36
NG_007376.1:g.294461A>G
NG_007376.2:g.294768A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000707132.1:n.2589A>G
ENST00000707133.1:n.1019A>G
ENST00000707134.1:n.1288A>G
ENST00000346798.8:c.*309A>G MANE Select	ENSP00000284981.4:n.*309A>G
ENST00000346798.7:c.*309A>G	ENSP00000284981.4:n.*309A>G
ENST00000348990.9:c.*309A>G	ENSP00000345463.5:n.*309A>G
ENST00000354192.7:c.*309A>G	ENSP00000346129.3:n.*309A>G
ENST00000357903.7:c.*309A>G	ENSP00000350578.3:n.*309A>G
ENST00000359726.7:c.*309A>G	ENSP00000352760.4:n.*309A>G
ENST00000439274.6:c.*309A>G	ENSP00000398879.2:n.*309A>G
ENST00000440126.7:c.*309A>G	ENSP00000387483.2:n.*309A>G
NM_000484.3:c.*309A>G	NP_000475.1:n.*309A>G
NM_001136016.3:c.*309A>G	NP_001129488.1:n.*309A>G
NM_001136129.2:c.*309A>G	NP_001129601.1:n.*309A>G
NM_001136130.2:c.*309A>G	NP_001129602.1:n.*309A>G
NM_001136131.2:c.*309A>G	NP_001129603.1:n.*309A>G
NM_001204301.1:c.*309A>G	NP_001191230.1:n.*309A>G
NM_001204302.1:c.*309A>G	NP_001191231.1:n.*309A>G
NM_001204303.1:c.*309A>G	NP_001191232.1:n.*309A>G
NM_201413.2:c.*309A>G	NP_958816.1:n.*309A>G
NM_201414.2:c.*309A>G	NP_958817.1:n.*309A>G
NM_000484.4:c.*309A>G MANE Select	NP_000475.1:n.*309A>G
NM_001136129.3:c.*309A>G	NP_001129601.1:n.*309A>G
NM_001136130.3:c.*309A>G	NP_001129602.1:n.*309A>G
NM_001204301.2:c.*309A>G	NP_001191230.1:n.*309A>G
NM_001204302.2:c.*309A>G	NP_001191231.1:n.*309A>G
NM_001204303.2:c.*309A>G	NP_001191232.1:n.*309A>G
NM_201413.3:c.*309A>G	NP_958816.1:n.*309A>G
NM_201414.3:c.*309A>G	NP_958817.1:n.*309A>G
NM_001136131.3:c.*309A>G	NP_001129603.1:n.*309A>G
NM_001385253.1:c.*309A>G	NP_001372182.1:n.*309A>G