Canonical Allele Identifier: CA1573508413
Gene: APC HGNC NCBI

Linked Data

dbSNP Id: rs1763997926

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112828800_112828803del , CM000667.2:g.112828800_112828803del GRCh38
NC_000005.9:g.112164497_112164500del , CM000667.1:g.112164497_112164500del GRCh37
NC_000005.8:g.112192396_112192399del NCBI36
NG_008481.4:g.141280_141283del , LRG_130:g.141280_141283del

Transcript Alleles

HGVS Amino-acid change
ENST00000257430.9:c.1627-56_1627-53del MANE Select ENSP00000257430.4:n.1627-56_1627-53del
ENST00000257430.8:c.1627-56_1627-53del ENSP00000257430.4:n.1627-56_1627-53del
ENST00000502371.2:n.97-6151_97-6148del
ENST00000504915.2:n.316-56_316-53del ENSP00000473355.1:n.316-56_316-53del
ENST00000505084.1:n.114-56_114-53del
ENST00000507379.5:c.1573-56_1573-53del ENSP00000423224.1:n.1573-56_1573-53del
ENST00000508376.6:c.1627-56_1627-53del ENSP00000427089.2:n.1627-56_1627-53del
ENST00000508624.5:c.*949-56_*949-53del ENSP00000424265.1:n.*949-56_*949-53del
ENST00000512211.6:c.1627-56_1627-53del ENSP00000423828.2:n.1627-56_1627-53del
ENST00000520401.1:n.114-56_114-53del
NM_000038.5:c.1627-56_1627-53del NP_000029.2:n.1627-56_1627-53del
NM_001127510.2:c.1627-56_1627-53del NP_001120982.1:n.1627-56_1627-53del
NM_001127511.2:c.1573-56_1573-53del NP_001120983.2:n.1573-56_1573-53del
NM_001354895.1:c.1627-56_1627-53del NP_001341824.1:n.1627-56_1627-53del
NM_001354896.1:c.1681-56_1681-53del NP_001341825.1:n.1681-56_1681-53del
NM_001354897.1:c.1657-56_1657-53del NP_001341826.1:n.1657-56_1657-53del
NM_001354898.1:c.1552-56_1552-53del NP_001341827.1:n.1552-56_1552-53del
NM_001354899.1:c.1543-56_1543-53del NP_001341828.1:n.1543-56_1543-53del
NM_001354900.1:c.1504-56_1504-53del NP_001341829.1:n.1504-56_1504-53del
NM_001354901.1:c.1450-56_1450-53del NP_001341830.1:n.1450-56_1450-53del
NM_001354902.1:c.1354-56_1354-53del NP_001341831.1:n.1354-56_1354-53del
NM_001354903.1:c.1324-56_1324-53del NP_001341832.1:n.1324-56_1324-53del
NM_001354904.1:c.1249-56_1249-53del NP_001341833.1:n.1249-56_1249-53del
NM_001354905.1:c.1147-56_1147-53del NP_001341834.1:n.1147-56_1147-53del
NM_001354906.1:c.778-56_778-53del NP_001341835.1:n.778-56_778-53del
NM_000038.6:c.1627-56_1627-53del MANE Select NP_000029.2:n.1627-56_1627-53del
NM_001127510.3:c.1627-56_1627-53del NP_001120982.1:n.1627-56_1627-53del
NM_001127511.3:c.1573-56_1573-53del NP_001120983.2:n.1573-56_1573-53del
NM_001354895.2:c.1627-56_1627-53del NP_001341824.1:n.1627-56_1627-53del
NM_001354896.2:c.1681-56_1681-53del NP_001341825.1:n.1681-56_1681-53del
NM_001354897.2:c.1657-56_1657-53del NP_001341826.1:n.1657-56_1657-53del
NM_001354898.2:c.1552-56_1552-53del NP_001341827.1:n.1552-56_1552-53del
NM_001354899.2:c.1543-56_1543-53del NP_001341828.1:n.1543-56_1543-53del
NM_001354900.2:c.1504-56_1504-53del NP_001341829.1:n.1504-56_1504-53del
NM_001354901.2:c.1450-56_1450-53del NP_001341830.1:n.1450-56_1450-53del
NM_001354902.2:c.1354-56_1354-53del NP_001341831.1:n.1354-56_1354-53del
NM_001354903.2:c.1324-56_1324-53del NP_001341832.1:n.1324-56_1324-53del
NM_001354904.2:c.1249-56_1249-53del NP_001341833.1:n.1249-56_1249-53del
NM_001354905.2:c.1147-56_1147-53del NP_001341834.1:n.1147-56_1147-53del
NM_001354906.2:c.778-56_778-53del NP_001341835.1:n.778-56_778-53del