Canonical Allele Identifier: CA409805500

Gene: APP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25891759T>G , CM000683.2:g.25891759T>G	GRCh38
NC_000021.8:g.27264071T>G , CM000683.1:g.27264071T>G	GRCh37
NC_000021.7:g.26185942T>G	NCBI36
NG_007376.1:g.284062A>C
NG_007376.2:g.284370A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000484.4:c.2174A>C MANE Select	NP_000475.1:p.Lys725Thr
ENST00000346798.8:c.2174A>C MANE Select	ENSP00000284981.4:p.Lys725Thr
NM_000484.3:c.2174A>C	NP_000475.1:p.Lys725Thr
NM_001136016.3:c.2102A>C	NP_001129488.1:p.Lys701Thr
NM_001136129.2:c.1781A>C	NP_001129601.1:p.Lys594Thr
NM_001136129.3:c.1781A>C	NP_001129601.1:p.Lys594Thr
NM_001136130.2:c.2006A>C	NP_001129602.1:p.Lys669Thr
NM_001136130.3:c.2006A>C	NP_001129602.1:p.Lys669Thr
NM_001136131.2:c.1844A>C	NP_001129603.1:p.Lys615Thr
NM_001136131.3:c.1844A>C	NP_001129603.1:p.Lys615Thr
NM_001204301.1:c.2120A>C	NP_001191230.1:p.Lys707Thr
NM_001204301.2:c.2120A>C	NP_001191230.1:p.Lys707Thr
NM_001204302.1:c.2063A>C	NP_001191231.1:p.Lys688Thr
NM_001204302.2:c.2063A>C	NP_001191231.1:p.Lys688Thr
NM_001204303.1:c.1895A>C	NP_001191232.1:p.Lys632Thr
NM_001204303.2:c.1895A>C	NP_001191232.1:p.Lys632Thr
NM_001385253.1:c.2006A>C	NP_001372182.1:p.Lys669Thr
NM_201413.2:c.2117A>C	NP_958816.1:p.Lys706Thr
NM_201413.3:c.2117A>C	NP_958816.1:p.Lys706Thr
NM_201414.2:c.1949A>C	NP_958817.1:p.Lys650Thr
NM_201414.3:c.1949A>C	NP_958817.1:p.Lys650Thr
ENST00000346798.7:c.2174A>C	ENSP00000284981.4:p.Lys725Thr
ENST00000348990.9:c.1949A>C	ENSP00000345463.5:p.Lys650Thr
ENST00000354192.7:c.1781A>C	ENSP00000346129.3:p.Lys594Thr
ENST00000357903.7:c.2117A>C	ENSP00000350578.3:p.Lys706Thr
ENST00000358918.7:c.2120A>C	ENSP00000351796.3:p.Lys707Thr
ENST00000359726.7:c.1844A>C	ENSP00000352760.4:p.Lys615Thr
ENST00000439274.6:c.2006A>C	ENSP00000398879.2:p.Lys669Thr
ENST00000440126.7:c.2102A>C	ENSP00000387483.2:p.Lys701Thr
ENST00000464867.1:n.521A>C
ENST00000707132.1:n.2141A>C
ENST00000707133.1:n.571A>C
ENST00000707134.1:n.840A>C