Canonical Allele Identifier: CA409806285

Gene: APP

Linked Data

• MyVariant Identifiers: chr21:g.27269901A>C (hg19) ; chr21:g.25897589A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25897589A>C , CM000683.2:g.25897589A>C	GRCh38
NC_000021.8:g.27269901A>C , CM000683.1:g.27269901A>C	GRCh37
NC_000021.7:g.26191772A>C	NCBI36
NG_007376.1:g.278232T>G
NG_007376.2:g.278540T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000707132.1:n.2015T>G
ENST00000707133.1:n.445T>G
ENST00000707134.1:n.714T>G
ENST00000346798.8:c.2048T>G MANE Select	ENSP00000284981.4:p.Val683Gly
ENST00000346798.7:c.2048T>G	ENSP00000284981.4:p.Val683Gly
ENST00000348990.9:c.1823T>G	ENSP00000345463.5:p.Val608Gly
ENST00000354192.7:c.1655T>G	ENSP00000346129.3:p.Val552Gly
ENST00000357903.7:c.1991T>G	ENSP00000350578.3:p.Val664Gly
ENST00000358918.7:c.1994T>G	ENSP00000351796.3:p.Val665Gly
ENST00000359726.7:c.1718T>G	ENSP00000352760.4:p.Val573Gly
ENST00000439274.6:c.1880T>G	ENSP00000398879.2:p.Val627Gly
ENST00000440126.7:c.1976T>G	ENSP00000387483.2:p.Val659Gly
ENST00000464867.1:n.395T>G
NM_000484.3:c.2048T>G	NP_000475.1:p.Val683Gly
NM_001136016.3:c.1976T>G	NP_001129488.1:p.Val659Gly
NM_001136129.2:c.1655T>G	NP_001129601.1:p.Val552Gly
NM_001136130.2:c.1880T>G	NP_001129602.1:p.Val627Gly
NM_001136131.2:c.1718T>G	NP_001129603.1:p.Val573Gly
NM_001204301.1:c.1994T>G	NP_001191230.1:p.Val665Gly
NM_001204302.1:c.1937T>G	NP_001191231.1:p.Val646Gly
NM_001204303.1:c.1769T>G	NP_001191232.1:p.Val590Gly
NM_201413.2:c.1991T>G	NP_958816.1:p.Val664Gly
NM_201414.2:c.1823T>G	NP_958817.1:p.Val608Gly
NM_000484.4:c.2048T>G MANE Select	NP_000475.1:p.Val683Gly
NM_001136129.3:c.1655T>G	NP_001129601.1:p.Val552Gly
NM_001136130.3:c.1880T>G	NP_001129602.1:p.Val627Gly
NM_001204301.2:c.1994T>G	NP_001191230.1:p.Val665Gly
NM_001204302.2:c.1937T>G	NP_001191231.1:p.Val646Gly
NM_001204303.2:c.1769T>G	NP_001191232.1:p.Val590Gly
NM_201413.3:c.1991T>G	NP_958816.1:p.Val664Gly
NM_201414.3:c.1823T>G	NP_958817.1:p.Val608Gly
NM_001136131.3:c.1718T>G	NP_001129603.1:p.Val573Gly
NM_001385253.1:c.1880T>G	NP_001372182.1:p.Val627Gly