Canonical Allele Identifier: CA1573475433
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112843603G= , CM000667.2:g.112843603G= GRCh38
NC_000005.9:g.112179300G= , CM000667.1:g.112179300G= GRCh37
NC_000005.8:g.112207199G= NCBI36
NG_008481.4:g.156083G= , LRG_130:g.156083G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000504915.3:c.8063G= ENSP00000473355.2:p.Arg2688=
ENST00000505350.2:c.*8015G= ENSP00000481752.1:n.*8015G=
ENST00000507379.6:c.7955G= ENSP00000423224.2:p.Arg2652=
ENST00000509732.6:c.8009G= ENSP00000426541.2:p.Arg2670=
ENST00000512211.7:c.8009G= ENSP00000423828.3:p.Arg2670=
ENST00000257430.9:c.8009G= MANE Select ENSP00000257430.4:p.Arg2670=
ENST00000257430.8:c.8009G= ENSP00000257430.4:p.Arg2670=
ENST00000508376.6:c.8009G= ENSP00000427089.2:p.Arg2670=
ENST00000520401.1:c.231-13046G=
NM_000038.5:c.8009G= NP_000029.2:p.Arg2670=
NM_001127510.2:c.8009G= NP_001120982.1:p.Arg2670=
NM_001127511.2:c.7955G= NP_001120983.2:p.Arg2652=
NM_001354895.1:c.8009G= NP_001341824.1:p.Arg2670=
NM_001354896.1:c.8063G= NP_001341825.1:p.Arg2688=
NM_001354897.1:c.8039G= NP_001341826.1:p.Arg2680=
NM_001354898.1:c.7934G= NP_001341827.1:p.Arg2645=
NM_001354899.1:c.7925G= NP_001341828.1:p.Arg2642=
NM_001354900.1:c.7886G= NP_001341829.1:p.Arg2629=
NM_001354901.1:c.7832G= NP_001341830.1:p.Arg2611=
NM_001354902.1:c.7736G= NP_001341831.1:p.Arg2579=
NM_001354903.1:c.7706G= NP_001341832.1:p.Arg2569=
NM_001354904.1:c.7631G= NP_001341833.1:p.Arg2544=
NM_001354905.1:c.7529G= NP_001341834.1:p.Arg2510=
NM_001354906.1:c.7160G= NP_001341835.1:p.Arg2387=
NM_000038.6:c.8009G= MANE Select NP_000029.2:p.Arg2670=
NM_001127510.3:c.8009G= NP_001120982.1:p.Arg2670=
NM_001127511.3:c.7955G= NP_001120983.2:p.Arg2652=
NM_001354895.2:c.8009G= NP_001341824.1:p.Arg2670=
NM_001354896.2:c.8063G= NP_001341825.1:p.Arg2688=
NM_001354897.2:c.8039G= NP_001341826.1:p.Arg2680=
NM_001354898.2:c.7934G= NP_001341827.1:p.Arg2645=
NM_001354899.2:c.7925G= NP_001341828.1:p.Arg2642=
NM_001354900.2:c.7886G= NP_001341829.1:p.Arg2629=
NM_001354901.2:c.7832G= NP_001341830.1:p.Arg2611=
NM_001354902.2:c.7736G= NP_001341831.1:p.Arg2579=
NM_001354903.2:c.7706G= NP_001341832.1:p.Arg2569=
NM_001354904.2:c.7631G= NP_001341833.1:p.Arg2544=
NM_001354905.2:c.7529G= NP_001341834.1:p.Arg2510=
NM_001354906.2:c.7160G= NP_001341835.1:p.Arg2387=