Canonical Allele Identifier: CA409806465

Gene: APP

Linked Data

• MyVariant Identifiers: chr21:g.27269943A>C (hg19) ; chr21:g.25897631A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25897631A>C , CM000683.2:g.25897631A>C	GRCh38
NC_000021.8:g.27269943A>C , CM000683.1:g.27269943A>C	GRCh37
NC_000021.7:g.26191814A>C	NCBI36
NG_007376.1:g.278190T>G
NG_007376.2:g.278498T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000707132.1:n.1973T>G
ENST00000707133.1:n.403T>G
ENST00000707134.1:n.672T>G
ENST00000346798.8:c.2006T>G MANE Select	ENSP00000284981.4:p.Val669Gly
ENST00000346798.7:c.2006T>G	ENSP00000284981.4:p.Val669Gly
ENST00000348990.9:c.1781T>G	ENSP00000345463.5:p.Val594Gly
ENST00000354192.7:c.1613T>G	ENSP00000346129.3:p.Val538Gly
ENST00000357903.7:c.1949T>G	ENSP00000350578.3:p.Val650Gly
ENST00000358918.7:c.1952T>G	ENSP00000351796.3:p.Val651Gly
ENST00000359726.7:c.1676T>G	ENSP00000352760.4:p.Val559Gly
ENST00000439274.6:c.1838T>G	ENSP00000398879.2:p.Val613Gly
ENST00000440126.7:c.1934T>G	ENSP00000387483.2:p.Val645Gly
ENST00000464867.1:n.353T>G
NM_000484.3:c.2006T>G	NP_000475.1:p.Val669Gly
NM_001136016.3:c.1934T>G	NP_001129488.1:p.Val645Gly
NM_001136129.2:c.1613T>G	NP_001129601.1:p.Val538Gly
NM_001136130.2:c.1838T>G	NP_001129602.1:p.Val613Gly
NM_001136131.2:c.1676T>G	NP_001129603.1:p.Val559Gly
NM_001204301.1:c.1952T>G	NP_001191230.1:p.Val651Gly
NM_001204302.1:c.1895T>G	NP_001191231.1:p.Val632Gly
NM_001204303.1:c.1727T>G	NP_001191232.1:p.Val576Gly
NM_201413.2:c.1949T>G	NP_958816.1:p.Val650Gly
NM_201414.2:c.1781T>G	NP_958817.1:p.Val594Gly
NM_000484.4:c.2006T>G MANE Select	NP_000475.1:p.Val669Gly
NM_001136129.3:c.1613T>G	NP_001129601.1:p.Val538Gly
NM_001136130.3:c.1838T>G	NP_001129602.1:p.Val613Gly
NM_001204301.2:c.1952T>G	NP_001191230.1:p.Val651Gly
NM_001204302.2:c.1895T>G	NP_001191231.1:p.Val632Gly
NM_001204303.2:c.1727T>G	NP_001191232.1:p.Val576Gly
NM_201413.3:c.1949T>G	NP_958816.1:p.Val650Gly
NM_201414.3:c.1781T>G	NP_958817.1:p.Val594Gly
NM_001136131.3:c.1676T>G	NP_001129603.1:p.Val559Gly
NM_001385253.1:c.1838T>G	NP_001372182.1:p.Val613Gly