Canonical Allele Identifier: CA409805621

Gene: APP

Linked Data

• MyVariant Identifiers: chr21:g.27264136A>C (hg19) ; chr21:g.25891824A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25891824A>C , CM000683.2:g.25891824A>C	GRCh38
NC_000021.8:g.27264136A>C , CM000683.1:g.27264136A>C	GRCh37
NC_000021.7:g.26186007A>C	NCBI36
NG_007376.1:g.283997T>G
NG_007376.2:g.284305T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000707132.1:n.2076T>G
ENST00000707133.1:n.506T>G
ENST00000707134.1:n.775T>G
ENST00000346798.8:c.2109T>G MANE Select	ENSP00000284981.4:p.Ile703Met
ENST00000346798.7:c.2109T>G	ENSP00000284981.4:p.Ile703Met
ENST00000348990.9:c.1884T>G	ENSP00000345463.5:p.Ile628Met
ENST00000354192.7:c.1716T>G	ENSP00000346129.3:p.Ile572Met
ENST00000357903.7:c.2052T>G	ENSP00000350578.3:p.Ile684Met
ENST00000358918.7:c.2055T>G	ENSP00000351796.3:p.Ile685Met
ENST00000359726.7:c.1779T>G	ENSP00000352760.4:p.Ile593Met
ENST00000439274.6:c.1941T>G	ENSP00000398879.2:p.Ile647Met
ENST00000440126.7:c.2037T>G	ENSP00000387483.2:p.Ile679Met
ENST00000464867.1:n.456T>G
NM_000484.3:c.2109T>G	NP_000475.1:p.Ile703Met
NM_001136016.3:c.2037T>G	NP_001129488.1:p.Ile679Met
NM_001136129.2:c.1716T>G	NP_001129601.1:p.Ile572Met
NM_001136130.2:c.1941T>G	NP_001129602.1:p.Ile647Met
NM_001136131.2:c.1779T>G	NP_001129603.1:p.Ile593Met
NM_001204301.1:c.2055T>G	NP_001191230.1:p.Ile685Met
NM_001204302.1:c.1998T>G	NP_001191231.1:p.Ile666Met
NM_001204303.1:c.1830T>G	NP_001191232.1:p.Ile610Met
NM_201413.2:c.2052T>G	NP_958816.1:p.Ile684Met
NM_201414.2:c.1884T>G	NP_958817.1:p.Ile628Met
NM_000484.4:c.2109T>G MANE Select	NP_000475.1:p.Ile703Met
NM_001136129.3:c.1716T>G	NP_001129601.1:p.Ile572Met
NM_001136130.3:c.1941T>G	NP_001129602.1:p.Ile647Met
NM_001204301.2:c.2055T>G	NP_001191230.1:p.Ile685Met
NM_001204302.2:c.1998T>G	NP_001191231.1:p.Ile666Met
NM_001204303.2:c.1830T>G	NP_001191232.1:p.Ile610Met
NM_201413.3:c.2052T>G	NP_958816.1:p.Ile684Met
NM_201414.3:c.1884T>G	NP_958817.1:p.Ile628Met
NM_001136131.3:c.1779T>G	NP_001129603.1:p.Ile593Met
NM_001385253.1:c.1941T>G	NP_001372182.1:p.Ile647Met