Canonical Allele Identifier: CA1573507916
Gene: APC HGNC NCBI

Linked Data

dbSNP Id: rs1763951789

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112828501_112828536del , CM000667.2:g.112828501_112828536del GRCh38
NC_000005.9:g.112164198_112164233del , CM000667.1:g.112164198_112164233del GRCh37
NC_000005.8:g.112192097_112192132del NCBI36
NG_008481.4:g.140981_141016del , LRG_130:g.140981_141016del

Transcript Alleles

HGVS Amino-acid change
ENST00000502371.3:c.1409-6450_1409-6415del ENSP00000484935.2:n.1409-6450_1409-6415del
ENST00000504915.3:c.1681-355_1681-320del ENSP00000473355.2:n.1681-355_1681-320del
ENST00000505084.2:n.1683-355_1683-320del
ENST00000505350.2:c.*1633-355_*1633-320del ENSP00000481752.1:n.*1633-355_*1633-320del
ENST00000507379.6:c.1573-355_1573-320del ENSP00000423224.2:n.1573-355_1573-320del
ENST00000509732.6:c.1627-355_1627-320del ENSP00000426541.2:n.1627-355_1627-320del
ENST00000512211.7:c.1627-355_1627-320del ENSP00000423828.3:n.1627-355_1627-320del
ENST00000257430.9:c.1627-355_1627-320del MANE Select ENSP00000257430.4:n.1627-355_1627-320del
ENST00000257430.8:c.1627-355_1627-320del ENSP00000257430.4:n.1627-355_1627-320del
ENST00000502371.2:c.97-6450_97-6415del
ENST00000504915.2:c.316-355_316-320del ENSP00000473355.1:n.316-355_316-320del
ENST00000505084.1:n.114-355_114-320del
ENST00000507379.5:c.1573-355_1573-320del ENSP00000423224.1:n.1573-355_1573-320del
ENST00000508376.6:c.1627-355_1627-320del ENSP00000427089.2:n.1627-355_1627-320del
ENST00000508624.5:c.*949-355_*949-320del ENSP00000424265.1:n.*949-355_*949-320del
ENST00000512211.6:c.1627-355_1627-320del ENSP00000423828.2:n.1627-355_1627-320del
ENST00000520401.1:c.114-355_114-320del
NM_000038.5:c.1627-355_1627-320del NP_000029.2:n.1627-355_1627-320del
NM_001127510.2:c.1627-355_1627-320del NP_001120982.1:n.1627-355_1627-320del
NM_001127511.2:c.1573-355_1573-320del NP_001120983.2:n.1573-355_1573-320del
NM_001354895.1:c.1627-355_1627-320del NP_001341824.1:n.1627-355_1627-320del
NM_001354896.1:c.1681-355_1681-320del NP_001341825.1:n.1681-355_1681-320del
NM_001354897.1:c.1657-355_1657-320del NP_001341826.1:n.1657-355_1657-320del
NM_001354898.1:c.1552-355_1552-320del NP_001341827.1:n.1552-355_1552-320del
NM_001354899.1:c.1543-355_1543-320del NP_001341828.1:n.1543-355_1543-320del
NM_001354900.1:c.1504-355_1504-320del NP_001341829.1:n.1504-355_1504-320del
NM_001354901.1:c.1450-355_1450-320del NP_001341830.1:n.1450-355_1450-320del
NM_001354902.1:c.1354-355_1354-320del NP_001341831.1:n.1354-355_1354-320del
NM_001354903.1:c.1324-355_1324-320del NP_001341832.1:n.1324-355_1324-320del
NM_001354904.1:c.1249-355_1249-320del NP_001341833.1:n.1249-355_1249-320del
NM_001354905.1:c.1147-355_1147-320del NP_001341834.1:n.1147-355_1147-320del
NM_001354906.1:c.778-355_778-320del NP_001341835.1:n.778-355_778-320del
NM_000038.6:c.1627-355_1627-320del MANE Select NP_000029.2:n.1627-355_1627-320del
NM_001127510.3:c.1627-355_1627-320del NP_001120982.1:n.1627-355_1627-320del
NM_001127511.3:c.1573-355_1573-320del NP_001120983.2:n.1573-355_1573-320del
NM_001354895.2:c.1627-355_1627-320del NP_001341824.1:n.1627-355_1627-320del
NM_001354896.2:c.1681-355_1681-320del NP_001341825.1:n.1681-355_1681-320del
NM_001354897.2:c.1657-355_1657-320del NP_001341826.1:n.1657-355_1657-320del
NM_001354898.2:c.1552-355_1552-320del NP_001341827.1:n.1552-355_1552-320del
NM_001354899.2:c.1543-355_1543-320del NP_001341828.1:n.1543-355_1543-320del
NM_001354900.2:c.1504-355_1504-320del NP_001341829.1:n.1504-355_1504-320del
NM_001354901.2:c.1450-355_1450-320del NP_001341830.1:n.1450-355_1450-320del
NM_001354902.2:c.1354-355_1354-320del NP_001341831.1:n.1354-355_1354-320del
NM_001354903.2:c.1324-355_1324-320del NP_001341832.1:n.1324-355_1324-320del
NM_001354904.2:c.1249-355_1249-320del NP_001341833.1:n.1249-355_1249-320del
NM_001354905.2:c.1147-355_1147-320del NP_001341834.1:n.1147-355_1147-320del
NM_001354906.2:c.778-355_778-320del NP_001341835.1:n.778-355_778-320del