Canonical Allele Identifier: CA748247473

Gene: APP

Linked Data

• dbSNP Id: rs1185060644
• MyVariant Identifiers: chr21:g.27269730_27269731insTATT (hg19) ; chr21:g.25897418_25897419insTATT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25897424_25897427dup , CM000683.2:g.25897424_25897427dup	GRCh38
NC_000021.8:g.27269736_27269739dup , CM000683.1:g.27269736_27269739dup	GRCh37
NC_000021.7:g.26191607_26191610dup	NCBI36
NG_007376.1:g.278399_278402dup
NG_007376.2:g.278707_278710dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000707132.1:n.2031+151_2031+154dup
ENST00000707133.1:n.461+151_461+154dup
ENST00000707134.1:n.730+151_730+154dup
ENST00000346798.8:c.2064+151_2064+154dup MANE Select	ENSP00000284981.4:n.2064+151_2064+154dup
ENST00000346798.7:c.2064+151_2064+154dup	ENSP00000284981.4:n.2064+151_2064+154dup
ENST00000348990.9:c.1839+151_1839+154dup	ENSP00000345463.5:n.1839+151_1839+154dup
ENST00000354192.7:c.1671+151_1671+154dup	ENSP00000346129.3:n.1671+151_1671+154dup
ENST00000357903.7:c.2007+151_2007+154dup	ENSP00000350578.3:n.2007+151_2007+154dup
ENST00000358918.7:c.2010+151_2010+154dup	ENSP00000351796.3:n.2010+151_2010+154dup
ENST00000359726.7:c.1734+151_1734+154dup	ENSP00000352760.4:n.1734+151_1734+154dup
ENST00000439274.6:c.1896+151_1896+154dup	ENSP00000398879.2:n.1896+151_1896+154dup
ENST00000440126.7:c.1992+151_1992+154dup	ENSP00000387483.2:n.1992+151_1992+154dup
ENST00000464867.1:n.411+151_411+154dup
NM_000484.3:c.2064+151_2064+154dup	NP_000475.1:n.2064+151_2064+154dup
NM_001136016.3:c.1992+151_1992+154dup	NP_001129488.1:n.1992+151_1992+154dup
NM_001136129.2:c.1671+151_1671+154dup	NP_001129601.1:n.1671+151_1671+154dup
NM_001136130.2:c.1896+151_1896+154dup	NP_001129602.1:n.1896+151_1896+154dup
NM_001136131.2:c.1734+151_1734+154dup	NP_001129603.1:n.1734+151_1734+154dup
NM_001204301.1:c.2010+151_2010+154dup	NP_001191230.1:n.2010+151_2010+154dup
NM_001204302.1:c.1953+151_1953+154dup	NP_001191231.1:n.1953+151_1953+154dup
NM_001204303.1:c.1785+151_1785+154dup	NP_001191232.1:n.1785+151_1785+154dup
NM_201413.2:c.2007+151_2007+154dup	NP_958816.1:n.2007+151_2007+154dup
NM_201414.2:c.1839+151_1839+154dup	NP_958817.1:n.1839+151_1839+154dup
NM_000484.4:c.2064+151_2064+154dup MANE Select	NP_000475.1:n.2064+151_2064+154dup
NM_001136129.3:c.1671+151_1671+154dup	NP_001129601.1:n.1671+151_1671+154dup
NM_001136130.3:c.1896+151_1896+154dup	NP_001129602.1:n.1896+151_1896+154dup
NM_001204301.2:c.2010+151_2010+154dup	NP_001191230.1:n.2010+151_2010+154dup
NM_001204302.2:c.1953+151_1953+154dup	NP_001191231.1:n.1953+151_1953+154dup
NM_001204303.2:c.1785+151_1785+154dup	NP_001191232.1:n.1785+151_1785+154dup
NM_201413.3:c.2007+151_2007+154dup	NP_958816.1:n.2007+151_2007+154dup
NM_201414.3:c.1839+151_1839+154dup	NP_958817.1:n.1839+151_1839+154dup
NM_001136131.3:c.1734+151_1734+154dup	NP_001129603.1:n.1734+151_1734+154dup
NM_001385253.1:c.1896+151_1896+154dup	NP_001372182.1:n.1896+151_1896+154dup