Canonical Allele Identifier: CA010734
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 185103
dbSNP Id: rs746346292

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112841433A>G , CM000667.2:g.112841433A>G GRCh38
NC_000005.9:g.112177130A>G , CM000667.1:g.112177130A>G GRCh37
NC_000005.8:g.112205029A>G NCBI36
NG_008481.4:g.153913A>G , LRG_130:g.153913A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000504915.3:c.5893A>G ENSP00000473355.2:p.Thr1965Ala
ENST00000505350.2:c.*5845A>G ENSP00000481752.1:n.*5845A>G
ENST00000507379.6:c.5785A>G ENSP00000423224.2:p.Thr1929Ala
ENST00000509732.6:c.5839A>G ENSP00000426541.2:p.Thr1947Ala
ENST00000512211.7:c.5839A>G ENSP00000423828.3:p.Thr1947Ala
ENST00000257430.9:c.5839A>G MANE Select ENSP00000257430.4:p.Thr1947Ala
ENST00000257430.8:c.5839A>G ENSP00000257430.4:p.Thr1947Ala
ENST00000508376.6:c.5839A>G ENSP00000427089.2:p.Thr1947Ala
ENST00000508624.5:c.*5161A>G ENSP00000424265.1:n.*5161A>G
ENST00000520401.1:c.230+12461A>G
NM_000038.5:c.5839A>G NP_000029.2:p.Thr1947Ala
NM_001127510.2:c.5839A>G NP_001120982.1:p.Thr1947Ala
NM_001127511.2:c.5785A>G NP_001120983.2:p.Thr1929Ala
NM_001354895.1:c.5839A>G NP_001341824.1:p.Thr1947Ala
NM_001354896.1:c.5893A>G NP_001341825.1:p.Thr1965Ala
NM_001354897.1:c.5869A>G NP_001341826.1:p.Thr1957Ala
NM_001354898.1:c.5764A>G NP_001341827.1:p.Thr1922Ala
NM_001354899.1:c.5755A>G NP_001341828.1:p.Thr1919Ala
NM_001354900.1:c.5716A>G NP_001341829.1:p.Thr1906Ala
NM_001354901.1:c.5662A>G NP_001341830.1:p.Thr1888Ala
NM_001354902.1:c.5566A>G NP_001341831.1:p.Thr1856Ala
NM_001354903.1:c.5536A>G NP_001341832.1:p.Thr1846Ala
NM_001354904.1:c.5461A>G NP_001341833.1:p.Thr1821Ala
NM_001354905.1:c.5359A>G NP_001341834.1:p.Thr1787Ala
NM_001354906.1:c.4990A>G NP_001341835.1:p.Thr1664Ala
NM_000038.6:c.5839A>G MANE Select NP_000029.2:p.Thr1947Ala
NM_001127510.3:c.5839A>G NP_001120982.1:p.Thr1947Ala
NM_001127511.3:c.5785A>G NP_001120983.2:p.Thr1929Ala
NM_001354895.2:c.5839A>G NP_001341824.1:p.Thr1947Ala
NM_001354896.2:c.5893A>G NP_001341825.1:p.Thr1965Ala
NM_001354897.2:c.5869A>G NP_001341826.1:p.Thr1957Ala
NM_001354898.2:c.5764A>G NP_001341827.1:p.Thr1922Ala
NM_001354899.2:c.5755A>G NP_001341828.1:p.Thr1919Ala
NM_001354900.2:c.5716A>G NP_001341829.1:p.Thr1906Ala
NM_001354901.2:c.5662A>G NP_001341830.1:p.Thr1888Ala
NM_001354902.2:c.5566A>G NP_001341831.1:p.Thr1856Ala
NM_001354903.2:c.5536A>G NP_001341832.1:p.Thr1846Ala
NM_001354904.2:c.5461A>G NP_001341833.1:p.Thr1821Ala
NM_001354905.2:c.5359A>G NP_001341834.1:p.Thr1787Ala
NM_001354906.2:c.4990A>G NP_001341835.1:p.Thr1664Ala