Canonical Allele Identifier: CA409806278

Gene: APP

Linked Data

• MyVariant Identifiers: chr21:g.27269899G>C (hg19) ; chr21:g.25897587G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25897587G>C , CM000683.2:g.25897587G>C	GRCh38
NC_000021.8:g.27269899G>C , CM000683.1:g.27269899G>C	GRCh37
NC_000021.7:g.26191770G>C	NCBI36
NG_007376.1:g.278234C>G
NG_007376.2:g.278542C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000707132.1:n.2017C>G
ENST00000707133.1:n.447C>G
ENST00000707134.1:n.716C>G
ENST00000346798.8:c.2050C>G MANE Select	ENSP00000284981.4:p.His684Asp
ENST00000346798.7:c.2050C>G	ENSP00000284981.4:p.His684Asp
ENST00000348990.9:c.1825C>G	ENSP00000345463.5:p.His609Asp
ENST00000354192.7:c.1657C>G	ENSP00000346129.3:p.His553Asp
ENST00000357903.7:c.1993C>G	ENSP00000350578.3:p.His665Asp
ENST00000358918.7:c.1996C>G	ENSP00000351796.3:p.His666Asp
ENST00000359726.7:c.1720C>G	ENSP00000352760.4:p.His574Asp
ENST00000439274.6:c.1882C>G	ENSP00000398879.2:p.His628Asp
ENST00000440126.7:c.1978C>G	ENSP00000387483.2:p.His660Asp
ENST00000464867.1:n.397C>G
NM_000484.3:c.2050C>G	NP_000475.1:p.His684Asp
NM_001136016.3:c.1978C>G	NP_001129488.1:p.His660Asp
NM_001136129.2:c.1657C>G	NP_001129601.1:p.His553Asp
NM_001136130.2:c.1882C>G	NP_001129602.1:p.His628Asp
NM_001136131.2:c.1720C>G	NP_001129603.1:p.His574Asp
NM_001204301.1:c.1996C>G	NP_001191230.1:p.His666Asp
NM_001204302.1:c.1939C>G	NP_001191231.1:p.His647Asp
NM_001204303.1:c.1771C>G	NP_001191232.1:p.His591Asp
NM_201413.2:c.1993C>G	NP_958816.1:p.His665Asp
NM_201414.2:c.1825C>G	NP_958817.1:p.His609Asp
NM_000484.4:c.2050C>G MANE Select	NP_000475.1:p.His684Asp
NM_001136129.3:c.1657C>G	NP_001129601.1:p.His553Asp
NM_001136130.3:c.1882C>G	NP_001129602.1:p.His628Asp
NM_001204301.2:c.1996C>G	NP_001191230.1:p.His666Asp
NM_001204302.2:c.1939C>G	NP_001191231.1:p.His647Asp
NM_001204303.2:c.1771C>G	NP_001191232.1:p.His591Asp
NM_201413.3:c.1993C>G	NP_958816.1:p.His665Asp
NM_201414.3:c.1825C>G	NP_958817.1:p.His609Asp
NM_001136131.3:c.1720C>G	NP_001129603.1:p.His574Asp
NM_001385253.1:c.1882C>G	NP_001372182.1:p.His628Asp