Canonical Allele Identifier: CA2654122936

Gene: APP

Linked Data

• gnomAD v4: 21-25897444-G-GTA

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25897445_25897446dup , CM000683.2:g.25897445_25897446dup	GRCh38
NC_000021.8:g.27269757_27269758dup , CM000683.1:g.27269757_27269758dup	GRCh37
NC_000021.7:g.26191628_26191629dup	NCBI36
NG_007376.1:g.278375_278376dup
NG_007376.2:g.278683_278684dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707132.1:n.2031+127_2031+128dup
ENST00000707133.1:n.461+127_461+128dup
ENST00000707134.1:n.730+127_730+128dup
ENST00000346798.8:c.2064+127_2064+128dup MANE Select	ENSP00000284981.4:n.2064+127_2064+128dup
ENST00000346798.7:c.2064+127_2064+128dup	ENSP00000284981.4:n.2064+127_2064+128dup
ENST00000348990.9:c.1839+127_1839+128dup	ENSP00000345463.5:n.1839+127_1839+128dup
ENST00000354192.7:c.1671+127_1671+128dup	ENSP00000346129.3:n.1671+127_1671+128dup
ENST00000357903.7:c.2007+127_2007+128dup	ENSP00000350578.3:n.2007+127_2007+128dup
ENST00000358918.7:c.2010+127_2010+128dup	ENSP00000351796.3:n.2010+127_2010+128dup
ENST00000359726.7:c.1734+127_1734+128dup	ENSP00000352760.4:n.1734+127_1734+128dup
ENST00000439274.6:c.1896+127_1896+128dup	ENSP00000398879.2:n.1896+127_1896+128dup
ENST00000440126.7:c.1992+127_1992+128dup	ENSP00000387483.2:n.1992+127_1992+128dup
ENST00000464867.1:n.411+127_411+128dup
NM_000484.3:c.2064+127_2064+128dup	NP_000475.1:n.2064+127_2064+128dup
NM_001136016.3:c.1992+127_1992+128dup	NP_001129488.1:n.1992+127_1992+128dup
NM_001136129.2:c.1671+127_1671+128dup	NP_001129601.1:n.1671+127_1671+128dup
NM_001136130.2:c.1896+127_1896+128dup	NP_001129602.1:n.1896+127_1896+128dup
NM_001136131.2:c.1734+127_1734+128dup	NP_001129603.1:n.1734+127_1734+128dup
NM_001204301.1:c.2010+127_2010+128dup	NP_001191230.1:n.2010+127_2010+128dup
NM_001204302.1:c.1953+127_1953+128dup	NP_001191231.1:n.1953+127_1953+128dup
NM_001204303.1:c.1785+127_1785+128dup	NP_001191232.1:n.1785+127_1785+128dup
NM_201413.2:c.2007+127_2007+128dup	NP_958816.1:n.2007+127_2007+128dup
NM_201414.2:c.1839+127_1839+128dup	NP_958817.1:n.1839+127_1839+128dup
NM_000484.4:c.2064+127_2064+128dup MANE Select	NP_000475.1:n.2064+127_2064+128dup
NM_001136129.3:c.1671+127_1671+128dup	NP_001129601.1:n.1671+127_1671+128dup
NM_001136130.3:c.1896+127_1896+128dup	NP_001129602.1:n.1896+127_1896+128dup
NM_001204301.2:c.2010+127_2010+128dup	NP_001191230.1:n.2010+127_2010+128dup
NM_001204302.2:c.1953+127_1953+128dup	NP_001191231.1:n.1953+127_1953+128dup
NM_001204303.2:c.1785+127_1785+128dup	NP_001191232.1:n.1785+127_1785+128dup
NM_201413.3:c.2007+127_2007+128dup	NP_958816.1:n.2007+127_2007+128dup
NM_201414.3:c.1839+127_1839+128dup	NP_958817.1:n.1839+127_1839+128dup
NM_001136131.3:c.1734+127_1734+128dup	NP_001129603.1:n.1734+127_1734+128dup
NM_001385253.1:c.1896+127_1896+128dup	NP_001372182.1:n.1896+127_1896+128dup