Canonical Allele Identifier: CA2737471590

Gene: APP

Linked Data

• dbSNP Id: rs2146263692

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25897422_25897423insGCC , CM000683.2:g.25897422_25897423insGCC	GRCh38
NC_000021.8:g.27269734_27269735insGCC , CM000683.1:g.27269734_27269735insGCC	GRCh37
NC_000021.7:g.26191605_26191606insGCC	NCBI36
NG_007376.1:g.278398_278399insGGC
NG_007376.2:g.278706_278707insGGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000707132.1:n.2031+150_2031+151insGGC
ENST00000707133.1:n.461+150_461+151insGGC
ENST00000707134.1:n.730+150_730+151insGGC
ENST00000346798.8:c.2064+150_2064+151insGGC MANE Select	ENSP00000284981.4:n.2064+150_2064+151insGGC
ENST00000346798.7:c.2064+150_2064+151insGGC	ENSP00000284981.4:n.2064+150_2064+151insGGC
ENST00000348990.9:c.1839+150_1839+151insGGC	ENSP00000345463.5:n.1839+150_1839+151insGGC
ENST00000354192.7:c.1671+150_1671+151insGGC	ENSP00000346129.3:n.1671+150_1671+151insGGC
ENST00000357903.7:c.2007+150_2007+151insGGC	ENSP00000350578.3:n.2007+150_2007+151insGGC
ENST00000358918.7:c.2010+150_2010+151insGGC	ENSP00000351796.3:n.2010+150_2010+151insGGC
ENST00000359726.7:c.1734+150_1734+151insGGC	ENSP00000352760.4:n.1734+150_1734+151insGGC
ENST00000439274.6:c.1896+150_1896+151insGGC	ENSP00000398879.2:n.1896+150_1896+151insGGC
ENST00000440126.7:c.1992+150_1992+151insGGC	ENSP00000387483.2:n.1992+150_1992+151insGGC
ENST00000464867.1:n.411+150_411+151insGGC
NM_000484.3:c.2064+150_2064+151insGGC	NP_000475.1:n.2064+150_2064+151insGGC
NM_001136016.3:c.1992+150_1992+151insGGC	NP_001129488.1:n.1992+150_1992+151insGGC
NM_001136129.2:c.1671+150_1671+151insGGC	NP_001129601.1:n.1671+150_1671+151insGGC
NM_001136130.2:c.1896+150_1896+151insGGC	NP_001129602.1:n.1896+150_1896+151insGGC
NM_001136131.2:c.1734+150_1734+151insGGC	NP_001129603.1:n.1734+150_1734+151insGGC
NM_001204301.1:c.2010+150_2010+151insGGC	NP_001191230.1:n.2010+150_2010+151insGGC
NM_001204302.1:c.1953+150_1953+151insGGC	NP_001191231.1:n.1953+150_1953+151insGGC
NM_001204303.1:c.1785+150_1785+151insGGC	NP_001191232.1:n.1785+150_1785+151insGGC
NM_201413.2:c.2007+150_2007+151insGGC	NP_958816.1:n.2007+150_2007+151insGGC
NM_201414.2:c.1839+150_1839+151insGGC	NP_958817.1:n.1839+150_1839+151insGGC
NM_000484.4:c.2064+150_2064+151insGGC MANE Select	NP_000475.1:n.2064+150_2064+151insGGC
NM_001136129.3:c.1671+150_1671+151insGGC	NP_001129601.1:n.1671+150_1671+151insGGC
NM_001136130.3:c.1896+150_1896+151insGGC	NP_001129602.1:n.1896+150_1896+151insGGC
NM_001204301.2:c.2010+150_2010+151insGGC	NP_001191230.1:n.2010+150_2010+151insGGC
NM_001204302.2:c.1953+150_1953+151insGGC	NP_001191231.1:n.1953+150_1953+151insGGC
NM_001204303.2:c.1785+150_1785+151insGGC	NP_001191232.1:n.1785+150_1785+151insGGC
NM_201413.3:c.2007+150_2007+151insGGC	NP_958816.1:n.2007+150_2007+151insGGC
NM_201414.3:c.1839+150_1839+151insGGC	NP_958817.1:n.1839+150_1839+151insGGC
NM_001136131.3:c.1734+150_1734+151insGGC	NP_001129603.1:n.1734+150_1734+151insGGC
NM_001385253.1:c.1896+150_1896+151insGGC	NP_001372182.1:n.1896+150_1896+151insGGC