Canonical Allele Identifier: CA1021425192

Gene: APP

Linked Data

• dbSNP Id: rs2038182527
• gnomAD v3: 21-25897860-AAAAG-A
• gnomAD v4: 21-25897860-AAAAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25897864_25897867del , CM000683.2:g.25897864_25897867del	GRCh38
NC_000021.8:g.27270176_27270179del , CM000683.1:g.27270176_27270179del	GRCh37
NC_000021.7:g.26192047_26192050del	NCBI36
NG_007376.1:g.277957_277960del
NG_007376.2:g.278265_278268del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707132.1:n.1931-191_1931-188del
ENST00000707133.1:n.361-191_361-188del
ENST00000707134.1:n.630-191_630-188del
ENST00000346798.8:c.1964-191_1964-188del MANE Select	ENSP00000284981.4:n.1964-191_1964-188del
ENST00000346798.7:c.1964-191_1964-188del	ENSP00000284981.4:n.1964-191_1964-188del
ENST00000348990.9:c.1739-191_1739-188del	ENSP00000345463.5:n.1739-191_1739-188del
ENST00000354192.7:c.1571-191_1571-188del	ENSP00000346129.3:n.1571-191_1571-188del
ENST00000357903.7:c.1907-191_1907-188del	ENSP00000350578.3:n.1907-191_1907-188del
ENST00000358918.7:c.1910-191_1910-188del	ENSP00000351796.3:n.1910-191_1910-188del
ENST00000359726.7:c.1634-191_1634-188del	ENSP00000352760.4:n.1634-191_1634-188del
ENST00000439274.6:c.1796-191_1796-188del	ENSP00000398879.2:n.1796-191_1796-188del
ENST00000440126.7:c.1892-191_1892-188del	ENSP00000387483.2:n.1892-191_1892-188del
ENST00000464867.1:n.120_123del
NM_000484.3:c.1964-191_1964-188del	NP_000475.1:n.1964-191_1964-188del
NM_001136016.3:c.1892-191_1892-188del	NP_001129488.1:n.1892-191_1892-188del
NM_001136129.2:c.1571-191_1571-188del	NP_001129601.1:n.1571-191_1571-188del
NM_001136130.2:c.1796-191_1796-188del	NP_001129602.1:n.1796-191_1796-188del
NM_001136131.2:c.1634-191_1634-188del	NP_001129603.1:n.1634-191_1634-188del
NM_001204301.1:c.1910-191_1910-188del	NP_001191230.1:n.1910-191_1910-188del
NM_001204302.1:c.1853-191_1853-188del	NP_001191231.1:n.1853-191_1853-188del
NM_001204303.1:c.1685-191_1685-188del	NP_001191232.1:n.1685-191_1685-188del
NM_201413.2:c.1907-191_1907-188del	NP_958816.1:n.1907-191_1907-188del
NM_201414.2:c.1739-191_1739-188del	NP_958817.1:n.1739-191_1739-188del
NM_000484.4:c.1964-191_1964-188del MANE Select	NP_000475.1:n.1964-191_1964-188del
NM_001136129.3:c.1571-191_1571-188del	NP_001129601.1:n.1571-191_1571-188del
NM_001136130.3:c.1796-191_1796-188del	NP_001129602.1:n.1796-191_1796-188del
NM_001204301.2:c.1910-191_1910-188del	NP_001191230.1:n.1910-191_1910-188del
NM_001204302.2:c.1853-191_1853-188del	NP_001191231.1:n.1853-191_1853-188del
NM_001204303.2:c.1685-191_1685-188del	NP_001191232.1:n.1685-191_1685-188del
NM_201413.3:c.1907-191_1907-188del	NP_958816.1:n.1907-191_1907-188del
NM_201414.3:c.1739-191_1739-188del	NP_958817.1:n.1739-191_1739-188del
NM_001136131.3:c.1634-191_1634-188del	NP_001129603.1:n.1634-191_1634-188del
NM_001385253.1:c.1796-191_1796-188del	NP_001372182.1:n.1796-191_1796-188del