Canonical Allele Identifier: CA2654122619

Gene: APP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25881337A>T , CM000683.2:g.25881337A>T	GRCh38
NC_000021.8:g.27253648A>T , CM000683.1:g.27253648A>T	GRCh37
NC_000021.7:g.26175519A>T	NCBI36
NG_007376.1:g.294485T>A
NG_007376.2:g.294792T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000484.4:c.*333T>A MANE Select	NP_000475.1:n.*333T>A
ENST00000346798.8:c.*333T>A MANE Select	ENSP00000284981.4:n.*333T>A
NM_000484.3:c.*333T>A	NP_000475.1:n.*333T>A
NM_001136016.3:c.*333T>A	NP_001129488.1:n.*333T>A
NM_001136129.2:c.*333T>A	NP_001129601.1:n.*333T>A
NM_001136129.3:c.*333T>A	NP_001129601.1:n.*333T>A
NM_001136130.2:c.*333T>A	NP_001129602.1:n.*333T>A
NM_001136130.3:c.*333T>A	NP_001129602.1:n.*333T>A
NM_001136131.2:c.*333T>A	NP_001129603.1:n.*333T>A
NM_001136131.3:c.*333T>A	NP_001129603.1:n.*333T>A
NM_001204301.1:c.*333T>A	NP_001191230.1:n.*333T>A
NM_001204301.2:c.*333T>A	NP_001191230.1:n.*333T>A
NM_001204302.1:c.*333T>A	NP_001191231.1:n.*333T>A
NM_001204302.2:c.*333T>A	NP_001191231.1:n.*333T>A
NM_001204303.1:c.*333T>A	NP_001191232.1:n.*333T>A
NM_001204303.2:c.*333T>A	NP_001191232.1:n.*333T>A
NM_001385253.1:c.*333T>A	NP_001372182.1:n.*333T>A
NM_201413.2:c.*333T>A	NP_958816.1:n.*333T>A
NM_201413.3:c.*333T>A	NP_958816.1:n.*333T>A
NM_201414.2:c.*333T>A	NP_958817.1:n.*333T>A
NM_201414.3:c.*333T>A	NP_958817.1:n.*333T>A
ENST00000346798.7:c.*333T>A	ENSP00000284981.4:n.*333T>A
ENST00000348990.9:c.*333T>A	ENSP00000345463.5:n.*333T>A
ENST00000354192.7:c.*333T>A	ENSP00000346129.3:n.*333T>A
ENST00000357903.7:c.*333T>A	ENSP00000350578.3:n.*333T>A
ENST00000359726.7:c.*333T>A	ENSP00000352760.4:n.*333T>A
ENST00000439274.6:c.*333T>A	ENSP00000398879.2:n.*333T>A
ENST00000440126.7:c.*333T>A	ENSP00000387483.2:n.*333T>A
ENST00000707132.1:n.2613T>A
ENST00000707133.1:n.1043T>A
ENST00000707134.1:n.1312T>A