Canonical Allele Identifier: CA409805657

Gene: APP

Linked Data

• MyVariant Identifiers: chr21:g.27264152T>G (hg19) ; chr21:g.25891840T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25891840T>G , CM000683.2:g.25891840T>G	GRCh38
NC_000021.8:g.27264152T>G , CM000683.1:g.27264152T>G	GRCh37
NC_000021.7:g.26186023T>G	NCBI36
NG_007376.1:g.283981A>C
NG_007376.2:g.284289A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000707132.1:n.2060A>C
ENST00000707133.1:n.490A>C
ENST00000707134.1:n.759A>C
ENST00000346798.8:c.2093A>C MANE Select	ENSP00000284981.4:p.Asn698Thr
ENST00000346798.7:c.2093A>C	ENSP00000284981.4:p.Asn698Thr
ENST00000348990.9:c.1868A>C	ENSP00000345463.5:p.Asn623Thr
ENST00000354192.7:c.1700A>C	ENSP00000346129.3:p.Asn567Thr
ENST00000357903.7:c.2036A>C	ENSP00000350578.3:p.Asn679Thr
ENST00000358918.7:c.2039A>C	ENSP00000351796.3:p.Asn680Thr
ENST00000359726.7:c.1763A>C	ENSP00000352760.4:p.Asn588Thr
ENST00000439274.6:c.1925A>C	ENSP00000398879.2:p.Asn642Thr
ENST00000440126.7:c.2021A>C	ENSP00000387483.2:p.Asn674Thr
ENST00000464867.1:n.440A>C
NM_000484.3:c.2093A>C	NP_000475.1:p.Asn698Thr
NM_001136016.3:c.2021A>C	NP_001129488.1:p.Asn674Thr
NM_001136129.2:c.1700A>C	NP_001129601.1:p.Asn567Thr
NM_001136130.2:c.1925A>C	NP_001129602.1:p.Asn642Thr
NM_001136131.2:c.1763A>C	NP_001129603.1:p.Asn588Thr
NM_001204301.1:c.2039A>C	NP_001191230.1:p.Asn680Thr
NM_001204302.1:c.1982A>C	NP_001191231.1:p.Asn661Thr
NM_001204303.1:c.1814A>C	NP_001191232.1:p.Asn605Thr
NM_201413.2:c.2036A>C	NP_958816.1:p.Asn679Thr
NM_201414.2:c.1868A>C	NP_958817.1:p.Asn623Thr
NM_000484.4:c.2093A>C MANE Select	NP_000475.1:p.Asn698Thr
NM_001136129.3:c.1700A>C	NP_001129601.1:p.Asn567Thr
NM_001136130.3:c.1925A>C	NP_001129602.1:p.Asn642Thr
NM_001204301.2:c.2039A>C	NP_001191230.1:p.Asn680Thr
NM_001204302.2:c.1982A>C	NP_001191231.1:p.Asn661Thr
NM_001204303.2:c.1814A>C	NP_001191232.1:p.Asn605Thr
NM_201413.3:c.2036A>C	NP_958816.1:p.Asn679Thr
NM_201414.3:c.1868A>C	NP_958817.1:p.Asn623Thr
NM_001136131.3:c.1763A>C	NP_001129603.1:p.Asn588Thr
NM_001385253.1:c.1925A>C	NP_001372182.1:p.Asn642Thr