Canonical Allele Identifier: CA409806342
Gene: APP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25897602A>G , CM000683.2:g.25897602A>G GRCh38
NC_000021.8:g.27269914A>G , CM000683.1:g.27269914A>G GRCh37
NC_000021.7:g.26191785A>G NCBI36
NG_007376.1:g.278219T>C
NG_007376.2:g.278527T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000707132.1:n.2002T>C
ENST00000707133.1:n.432T>C
ENST00000707134.1:n.701T>C
ENST00000346798.8:c.2035T>C MANE Select ENSP00000284981.4:p.Ser679Pro
ENST00000346798.7:c.2035T>C ENSP00000284981.4:p.Ser679Pro
ENST00000348990.9:c.1810T>C ENSP00000345463.5:p.Ser604Pro
ENST00000354192.7:c.1642T>C ENSP00000346129.3:p.Ser548Pro
ENST00000357903.7:c.1978T>C ENSP00000350578.3:p.Ser660Pro
ENST00000358918.7:c.1981T>C ENSP00000351796.3:p.Ser661Pro
ENST00000359726.7:c.1705T>C ENSP00000352760.4:p.Ser569Pro
ENST00000439274.6:c.1867T>C ENSP00000398879.2:p.Ser623Pro
ENST00000440126.7:c.1963T>C ENSP00000387483.2:p.Ser655Pro
ENST00000464867.1:n.382T>C
NM_000484.3:c.2035T>C NP_000475.1:p.Ser679Pro
NM_001136016.3:c.1963T>C NP_001129488.1:p.Ser655Pro
NM_001136129.2:c.1642T>C NP_001129601.1:p.Ser548Pro
NM_001136130.2:c.1867T>C NP_001129602.1:p.Ser623Pro
NM_001136131.2:c.1705T>C NP_001129603.1:p.Ser569Pro
NM_001204301.1:c.1981T>C NP_001191230.1:p.Ser661Pro
NM_001204302.1:c.1924T>C NP_001191231.1:p.Ser642Pro
NM_001204303.1:c.1756T>C NP_001191232.1:p.Ser586Pro
NM_201413.2:c.1978T>C NP_958816.1:p.Ser660Pro
NM_201414.2:c.1810T>C NP_958817.1:p.Ser604Pro
NM_000484.4:c.2035T>C MANE Select NP_000475.1:p.Ser679Pro
NM_001136129.3:c.1642T>C NP_001129601.1:p.Ser548Pro
NM_001136130.3:c.1867T>C NP_001129602.1:p.Ser623Pro
NM_001204301.2:c.1981T>C NP_001191230.1:p.Ser661Pro
NM_001204302.2:c.1924T>C NP_001191231.1:p.Ser642Pro
NM_001204303.2:c.1756T>C NP_001191232.1:p.Ser586Pro
NM_201413.3:c.1978T>C NP_958816.1:p.Ser660Pro
NM_201414.3:c.1810T>C NP_958817.1:p.Ser604Pro
NM_001136131.3:c.1705T>C NP_001129603.1:p.Ser569Pro
NM_001385253.1:c.1867T>C NP_001372182.1:p.Ser623Pro