Canonical Allele Identifier: CA409806256

Gene: APP

Linked Data

• MyVariant Identifiers: chr21:g.27269895T>G (hg19) ; chr21:g.25897583T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25897583T>G , CM000683.2:g.25897583T>G	GRCh38
NC_000021.8:g.27269895T>G , CM000683.1:g.27269895T>G	GRCh37
NC_000021.7:g.26191766T>G	NCBI36
NG_007376.1:g.278238A>C
NG_007376.2:g.278546A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000707132.1:n.2021A>C
ENST00000707133.1:n.451A>C
ENST00000707134.1:n.720A>C
ENST00000346798.8:c.2054A>C MANE Select	ENSP00000284981.4:p.His685Pro
ENST00000346798.7:c.2054A>C	ENSP00000284981.4:p.His685Pro
ENST00000348990.9:c.1829A>C	ENSP00000345463.5:p.His610Pro
ENST00000354192.7:c.1661A>C	ENSP00000346129.3:p.His554Pro
ENST00000357903.7:c.1997A>C	ENSP00000350578.3:p.His666Pro
ENST00000358918.7:c.2000A>C	ENSP00000351796.3:p.His667Pro
ENST00000359726.7:c.1724A>C	ENSP00000352760.4:p.His575Pro
ENST00000439274.6:c.1886A>C	ENSP00000398879.2:p.His629Pro
ENST00000440126.7:c.1982A>C	ENSP00000387483.2:p.His661Pro
ENST00000464867.1:n.401A>C
NM_000484.3:c.2054A>C	NP_000475.1:p.His685Pro
NM_001136016.3:c.1982A>C	NP_001129488.1:p.His661Pro
NM_001136129.2:c.1661A>C	NP_001129601.1:p.His554Pro
NM_001136130.2:c.1886A>C	NP_001129602.1:p.His629Pro
NM_001136131.2:c.1724A>C	NP_001129603.1:p.His575Pro
NM_001204301.1:c.2000A>C	NP_001191230.1:p.His667Pro
NM_001204302.1:c.1943A>C	NP_001191231.1:p.His648Pro
NM_001204303.1:c.1775A>C	NP_001191232.1:p.His592Pro
NM_201413.2:c.1997A>C	NP_958816.1:p.His666Pro
NM_201414.2:c.1829A>C	NP_958817.1:p.His610Pro
NM_000484.4:c.2054A>C MANE Select	NP_000475.1:p.His685Pro
NM_001136129.3:c.1661A>C	NP_001129601.1:p.His554Pro
NM_001136130.3:c.1886A>C	NP_001129602.1:p.His629Pro
NM_001204301.2:c.2000A>C	NP_001191230.1:p.His667Pro
NM_001204302.2:c.1943A>C	NP_001191231.1:p.His648Pro
NM_001204303.2:c.1775A>C	NP_001191232.1:p.His592Pro
NM_201413.3:c.1997A>C	NP_958816.1:p.His666Pro
NM_201414.3:c.1829A>C	NP_958817.1:p.His610Pro
NM_001136131.3:c.1724A>C	NP_001129603.1:p.His575Pro
NM_001385253.1:c.1886A>C	NP_001372182.1:p.His629Pro