Canonical Allele Identifier: CA16024882
Gene: APC HGNC NCBI

Linked Data

dbSNP Id: rs2149816929

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112828865A>T , CM000667.2:g.112828865A>T GRCh38
NC_000005.9:g.112164562A>T , CM000667.1:g.112164562A>T GRCh37
NC_000005.8:g.112192461A>T NCBI36
NG_008481.4:g.141345A>T , LRG_130:g.141345A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000502371.3:c.1409-6086A>T ENSP00000484935.2:n.1409-6086A>T
ENST00000504915.3:c.1690A>T ENSP00000473355.2:p.Ser564Cys
ENST00000505084.2:n.1692A>T
ENST00000505350.2:c.*1642A>T ENSP00000481752.1:n.*1642A>T
ENST00000507379.6:c.1582A>T ENSP00000423224.2:p.Ser528Cys
ENST00000509732.6:c.1636A>T ENSP00000426541.2:p.Ser546Cys
ENST00000512211.7:c.1636A>T ENSP00000423828.3:p.Ser546Cys
ENST00000257430.9:c.1636A>T MANE Select ENSP00000257430.4:p.Ser546Cys
ENST00000257430.8:c.1636A>T ENSP00000257430.4:p.Ser546Cys
ENST00000502371.2:c.97-6086A>T
ENST00000504915.2:c.325A>T ENSP00000473355.1:p.Ser109Cys
ENST00000505084.1:n.123A>T
ENST00000507379.5:c.1582A>T ENSP00000423224.1:p.Ser528Cys
ENST00000508376.6:c.1636A>T ENSP00000427089.2:p.Ser546Cys
ENST00000508624.5:c.*958A>T ENSP00000424265.1:n.*958A>T
ENST00000512211.6:c.1636A>T ENSP00000423828.2:p.Ser546Cys
ENST00000520401.1:c.123A>T
NM_000038.5:c.1636A>T NP_000029.2:p.Ser546Cys
NM_001127510.2:c.1636A>T NP_001120982.1:p.Ser546Cys
NM_001127511.2:c.1582A>T NP_001120983.2:p.Ser528Cys
NM_001354895.1:c.1636A>T NP_001341824.1:p.Ser546Cys
NM_001354896.1:c.1690A>T NP_001341825.1:p.Ser564Cys
NM_001354897.1:c.1666A>T NP_001341826.1:p.Ser556Cys
NM_001354898.1:c.1561A>T NP_001341827.1:p.Ser521Cys
NM_001354899.1:c.1552A>T NP_001341828.1:p.Ser518Cys
NM_001354900.1:c.1513A>T NP_001341829.1:p.Ser505Cys
NM_001354901.1:c.1459A>T NP_001341830.1:p.Ser487Cys
NM_001354902.1:c.1363A>T NP_001341831.1:p.Ser455Cys
NM_001354903.1:c.1333A>T NP_001341832.1:p.Ser445Cys
NM_001354904.1:c.1258A>T NP_001341833.1:p.Ser420Cys
NM_001354905.1:c.1156A>T NP_001341834.1:p.Ser386Cys
NM_001354906.1:c.787A>T NP_001341835.1:p.Ser263Cys
NM_000038.6:c.1636A>T MANE Select NP_000029.2:p.Ser546Cys
NM_001127510.3:c.1636A>T NP_001120982.1:p.Ser546Cys
NM_001127511.3:c.1582A>T NP_001120983.2:p.Ser528Cys
NM_001354895.2:c.1636A>T NP_001341824.1:p.Ser546Cys
NM_001354896.2:c.1690A>T NP_001341825.1:p.Ser564Cys
NM_001354897.2:c.1666A>T NP_001341826.1:p.Ser556Cys
NM_001354898.2:c.1561A>T NP_001341827.1:p.Ser521Cys
NM_001354899.2:c.1552A>T NP_001341828.1:p.Ser518Cys
NM_001354900.2:c.1513A>T NP_001341829.1:p.Ser505Cys
NM_001354901.2:c.1459A>T NP_001341830.1:p.Ser487Cys
NM_001354902.2:c.1363A>T NP_001341831.1:p.Ser455Cys
NM_001354903.2:c.1333A>T NP_001341832.1:p.Ser445Cys
NM_001354904.2:c.1258A>T NP_001341833.1:p.Ser420Cys
NM_001354905.2:c.1156A>T NP_001341834.1:p.Ser386Cys
NM_001354906.2:c.787A>T NP_001341835.1:p.Ser263Cys