Canonical Allele Identifier: CA1573475568
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112840911A= , CM000667.2:g.112840911A= GRCh38
NC_000005.9:g.112176608A= , CM000667.1:g.112176608A= GRCh37
NC_000005.8:g.112204507A= NCBI36
NG_008481.4:g.153391A= , LRG_130:g.153391A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000504915.3:c.5371A= ENSP00000473355.2:p.Thr1791=
ENST00000505350.2:c.*5323A= ENSP00000481752.1:n.*5323A=
ENST00000507379.6:c.5263A= ENSP00000423224.2:p.Thr1755=
ENST00000509732.6:c.5317A= ENSP00000426541.2:p.Thr1773=
ENST00000512211.7:c.5317A= ENSP00000423828.3:p.Thr1773=
ENST00000257430.9:c.5317A= MANE Select ENSP00000257430.4:p.Thr1773=
ENST00000257430.8:c.5317A= ENSP00000257430.4:p.Thr1773=
ENST00000508376.6:c.5317A= ENSP00000427089.2:p.Thr1773=
ENST00000508624.5:c.*4639A= ENSP00000424265.1:n.*4639A=
ENST00000520401.1:c.230+11939A=
NM_000038.5:c.5317A= NP_000029.2:p.Thr1773=
NM_001127510.2:c.5317A= NP_001120982.1:p.Thr1773=
NM_001127511.2:c.5263A= NP_001120983.2:p.Thr1755=
NM_001354895.1:c.5317A= NP_001341824.1:p.Thr1773=
NM_001354896.1:c.5371A= NP_001341825.1:p.Thr1791=
NM_001354897.1:c.5347A= NP_001341826.1:p.Thr1783=
NM_001354898.1:c.5242A= NP_001341827.1:p.Thr1748=
NM_001354899.1:c.5233A= NP_001341828.1:p.Thr1745=
NM_001354900.1:c.5194A= NP_001341829.1:p.Thr1732=
NM_001354901.1:c.5140A= NP_001341830.1:p.Thr1714=
NM_001354902.1:c.5044A= NP_001341831.1:p.Thr1682=
NM_001354903.1:c.5014A= NP_001341832.1:p.Thr1672=
NM_001354904.1:c.4939A= NP_001341833.1:p.Thr1647=
NM_001354905.1:c.4837A= NP_001341834.1:p.Thr1613=
NM_001354906.1:c.4468A= NP_001341835.1:p.Thr1490=
NM_000038.6:c.5317A= MANE Select NP_000029.2:p.Thr1773=
NM_001127510.3:c.5317A= NP_001120982.1:p.Thr1773=
NM_001127511.3:c.5263A= NP_001120983.2:p.Thr1755=
NM_001354895.2:c.5317A= NP_001341824.1:p.Thr1773=
NM_001354896.2:c.5371A= NP_001341825.1:p.Thr1791=
NM_001354897.2:c.5347A= NP_001341826.1:p.Thr1783=
NM_001354898.2:c.5242A= NP_001341827.1:p.Thr1748=
NM_001354899.2:c.5233A= NP_001341828.1:p.Thr1745=
NM_001354900.2:c.5194A= NP_001341829.1:p.Thr1732=
NM_001354901.2:c.5140A= NP_001341830.1:p.Thr1714=
NM_001354902.2:c.5044A= NP_001341831.1:p.Thr1682=
NM_001354903.2:c.5014A= NP_001341832.1:p.Thr1672=
NM_001354904.2:c.4939A= NP_001341833.1:p.Thr1647=
NM_001354905.2:c.4837A= NP_001341834.1:p.Thr1613=
NM_001354906.2:c.4468A= NP_001341835.1:p.Thr1490=