Canonical Allele Identifier: CA16033423
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470012
dbSNP Id: rs1461006300

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112841121C>A , CM000667.2:g.112841121C>A GRCh38
NC_000005.9:g.112176818C>A , CM000667.1:g.112176818C>A GRCh37
NC_000005.8:g.112204717C>A NCBI36
NG_008481.4:g.153601C>A , LRG_130:g.153601C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000504915.3:c.5581C>A ENSP00000473355.2:p.Pro1861Thr
ENST00000505350.2:c.*5533C>A ENSP00000481752.1:n.*5533C>A
ENST00000507379.6:c.5473C>A ENSP00000423224.2:p.Pro1825Thr
ENST00000509732.6:c.5527C>A ENSP00000426541.2:p.Pro1843Thr
ENST00000512211.7:c.5527C>A ENSP00000423828.3:p.Pro1843Thr
ENST00000257430.9:c.5527C>A MANE Select ENSP00000257430.4:p.Pro1843Thr
ENST00000257430.8:c.5527C>A ENSP00000257430.4:p.Pro1843Thr
ENST00000508376.6:c.5527C>A ENSP00000427089.2:p.Pro1843Thr
ENST00000508624.5:c.*4849C>A ENSP00000424265.1:n.*4849C>A
ENST00000520401.1:c.230+12149C>A
NM_000038.5:c.5527C>A NP_000029.2:p.Pro1843Thr
NM_001127510.2:c.5527C>A NP_001120982.1:p.Pro1843Thr
NM_001127511.2:c.5473C>A NP_001120983.2:p.Pro1825Thr
NM_001354895.1:c.5527C>A NP_001341824.1:p.Pro1843Thr
NM_001354896.1:c.5581C>A NP_001341825.1:p.Pro1861Thr
NM_001354897.1:c.5557C>A NP_001341826.1:p.Pro1853Thr
NM_001354898.1:c.5452C>A NP_001341827.1:p.Pro1818Thr
NM_001354899.1:c.5443C>A NP_001341828.1:p.Pro1815Thr
NM_001354900.1:c.5404C>A NP_001341829.1:p.Pro1802Thr
NM_001354901.1:c.5350C>A NP_001341830.1:p.Pro1784Thr
NM_001354902.1:c.5254C>A NP_001341831.1:p.Pro1752Thr
NM_001354903.1:c.5224C>A NP_001341832.1:p.Pro1742Thr
NM_001354904.1:c.5149C>A NP_001341833.1:p.Pro1717Thr
NM_001354905.1:c.5047C>A NP_001341834.1:p.Pro1683Thr
NM_001354906.1:c.4678C>A NP_001341835.1:p.Pro1560Thr
NM_000038.6:c.5527C>A MANE Select NP_000029.2:p.Pro1843Thr
NM_001127510.3:c.5527C>A NP_001120982.1:p.Pro1843Thr
NM_001127511.3:c.5473C>A NP_001120983.2:p.Pro1825Thr
NM_001354895.2:c.5527C>A NP_001341824.1:p.Pro1843Thr
NM_001354896.2:c.5581C>A NP_001341825.1:p.Pro1861Thr
NM_001354897.2:c.5557C>A NP_001341826.1:p.Pro1853Thr
NM_001354898.2:c.5452C>A NP_001341827.1:p.Pro1818Thr
NM_001354899.2:c.5443C>A NP_001341828.1:p.Pro1815Thr
NM_001354900.2:c.5404C>A NP_001341829.1:p.Pro1802Thr
NM_001354901.2:c.5350C>A NP_001341830.1:p.Pro1784Thr
NM_001354902.2:c.5254C>A NP_001341831.1:p.Pro1752Thr
NM_001354903.2:c.5224C>A NP_001341832.1:p.Pro1742Thr
NM_001354904.2:c.5149C>A NP_001341833.1:p.Pro1717Thr
NM_001354905.2:c.5047C>A NP_001341834.1:p.Pro1683Thr
NM_001354906.2:c.4678C>A NP_001341835.1:p.Pro1560Thr