Canonical Allele Identifier: CA1573470753
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112843036C= , CM000667.2:g.112843036C= GRCh38
NC_000005.9:g.112178733C= , CM000667.1:g.112178733C= GRCh37
NC_000005.8:g.112206632C= NCBI36
NG_008481.4:g.155516C= , LRG_130:g.155516C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000504915.3:c.7496C= ENSP00000473355.2:p.Thr2499=
ENST00000505350.2:c.*7448C= ENSP00000481752.1:n.*7448C=
ENST00000507379.6:c.7388C= ENSP00000423224.2:p.Thr2463=
ENST00000509732.6:c.7442C= ENSP00000426541.2:p.Thr2481=
ENST00000512211.7:c.7442C= ENSP00000423828.3:p.Thr2481=
ENST00000257430.9:c.7442C= MANE Select ENSP00000257430.4:p.Thr2481=
ENST00000257430.8:c.7442C= ENSP00000257430.4:p.Thr2481=
ENST00000508376.6:c.7442C= ENSP00000427089.2:p.Thr2481=
ENST00000520401.1:c.231-13613C=
NM_000038.5:c.7442C= NP_000029.2:p.Thr2481=
NM_001127510.2:c.7442C= NP_001120982.1:p.Thr2481=
NM_001127511.2:c.7388C= NP_001120983.2:p.Thr2463=
NM_001354895.1:c.7442C= NP_001341824.1:p.Thr2481=
NM_001354896.1:c.7496C= NP_001341825.1:p.Thr2499=
NM_001354897.1:c.7472C= NP_001341826.1:p.Thr2491=
NM_001354898.1:c.7367C= NP_001341827.1:p.Thr2456=
NM_001354899.1:c.7358C= NP_001341828.1:p.Thr2453=
NM_001354900.1:c.7319C= NP_001341829.1:p.Thr2440=
NM_001354901.1:c.7265C= NP_001341830.1:p.Thr2422=
NM_001354902.1:c.7169C= NP_001341831.1:p.Thr2390=
NM_001354903.1:c.7139C= NP_001341832.1:p.Thr2380=
NM_001354904.1:c.7064C= NP_001341833.1:p.Thr2355=
NM_001354905.1:c.6962C= NP_001341834.1:p.Thr2321=
NM_001354906.1:c.6593C= NP_001341835.1:p.Thr2198=
NM_000038.6:c.7442C= MANE Select NP_000029.2:p.Thr2481=
NM_001127510.3:c.7442C= NP_001120982.1:p.Thr2481=
NM_001127511.3:c.7388C= NP_001120983.2:p.Thr2463=
NM_001354895.2:c.7442C= NP_001341824.1:p.Thr2481=
NM_001354896.2:c.7496C= NP_001341825.1:p.Thr2499=
NM_001354897.2:c.7472C= NP_001341826.1:p.Thr2491=
NM_001354898.2:c.7367C= NP_001341827.1:p.Thr2456=
NM_001354899.2:c.7358C= NP_001341828.1:p.Thr2453=
NM_001354900.2:c.7319C= NP_001341829.1:p.Thr2440=
NM_001354901.2:c.7265C= NP_001341830.1:p.Thr2422=
NM_001354902.2:c.7169C= NP_001341831.1:p.Thr2390=
NM_001354903.2:c.7139C= NP_001341832.1:p.Thr2380=
NM_001354904.2:c.7064C= NP_001341833.1:p.Thr2355=
NM_001354905.2:c.6962C= NP_001341834.1:p.Thr2321=
NM_001354906.2:c.6593C= NP_001341835.1:p.Thr2198=