Canonical Allele Identifier: CA511686037

Gene: APP

Linked Data

• MyVariant Identifiers: chr21:g.27264154T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25891842T>G , CM000683.2:g.25891842T>G	GRCh38
NC_000021.8:g.27264154T>G , CM000683.1:g.27264154T>G	GRCh37
NC_000021.7:g.26186025T>G	NCBI36
NG_007376.1:g.283979A>C
NG_007376.2:g.284287A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000707132.1:n.2058A>C
ENST00000707133.1:n.488A>C
ENST00000707134.1:n.757A>C
ENST00000346798.8:c.2091A>C MANE Select	ENSP00000284981.4:p.Ser697=
ENST00000346798.7:c.2091A>C	ENSP00000284981.4:p.Ser697=
ENST00000348990.9:c.1866A>C	ENSP00000345463.5:p.Ser622=
ENST00000354192.7:c.1698A>C	ENSP00000346129.3:p.Ser566=
ENST00000357903.7:c.2034A>C	ENSP00000350578.3:p.Ser678=
ENST00000358918.7:c.2037A>C	ENSP00000351796.3:p.Ser679=
ENST00000359726.7:c.1761A>C	ENSP00000352760.4:p.Ser587=
ENST00000439274.6:c.1923A>C	ENSP00000398879.2:p.Ser641=
ENST00000440126.7:c.2019A>C	ENSP00000387483.2:p.Ser673=
ENST00000464867.1:n.438A>C
NM_000484.3:c.2091A>C	NP_000475.1:p.Ser697=
NM_001136016.3:c.2019A>C	NP_001129488.1:p.Ser673=
NM_001136129.2:c.1698A>C	NP_001129601.1:p.Ser566=
NM_001136130.2:c.1923A>C	NP_001129602.1:p.Ser641=
NM_001136131.2:c.1761A>C	NP_001129603.1:p.Ser587=
NM_001204301.1:c.2037A>C	NP_001191230.1:p.Ser679=
NM_001204302.1:c.1980A>C	NP_001191231.1:p.Ser660=
NM_001204303.1:c.1812A>C	NP_001191232.1:p.Ser604=
NM_201413.2:c.2034A>C	NP_958816.1:p.Ser678=
NM_201414.2:c.1866A>C	NP_958817.1:p.Ser622=
NM_000484.4:c.2091A>C MANE Select	NP_000475.1:p.Ser697=
NM_001136129.3:c.1698A>C	NP_001129601.1:p.Ser566=
NM_001136130.3:c.1923A>C	NP_001129602.1:p.Ser641=
NM_001204301.2:c.2037A>C	NP_001191230.1:p.Ser679=
NM_001204302.2:c.1980A>C	NP_001191231.1:p.Ser660=
NM_001204303.2:c.1812A>C	NP_001191232.1:p.Ser604=
NM_201413.3:c.2034A>C	NP_958816.1:p.Ser678=
NM_201414.3:c.1866A>C	NP_958817.1:p.Ser622=
NM_001136131.3:c.1761A>C	NP_001129603.1:p.Ser587=
NM_001385253.1:c.1923A>C	NP_001372182.1:p.Ser641=