Canonical Allele Identifier: CA1573475542
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112843619C= , CM000667.2:g.112843619C= GRCh38
NC_000005.9:g.112179316C= , CM000667.1:g.112179316C= GRCh37
NC_000005.8:g.112207215C= NCBI36
NG_008481.4:g.156099C= , LRG_130:g.156099C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000504915.3:c.8079C= ENSP00000473355.2:p.Pro2693=
ENST00000505350.2:c.*8031C= ENSP00000481752.1:n.*8031C=
ENST00000507379.6:c.7971C= ENSP00000423224.2:p.Pro2657=
ENST00000509732.6:c.8025C= ENSP00000426541.2:p.Pro2675=
ENST00000512211.7:c.8025C= ENSP00000423828.3:p.Pro2675=
ENST00000257430.9:c.8025C= MANE Select ENSP00000257430.4:p.Pro2675=
ENST00000257430.8:c.8025C= ENSP00000257430.4:p.Pro2675=
ENST00000508376.6:c.8025C= ENSP00000427089.2:p.Pro2675=
ENST00000520401.1:c.231-13030C=
NM_000038.5:c.8025C= NP_000029.2:p.Pro2675=
NM_001127510.2:c.8025C= NP_001120982.1:p.Pro2675=
NM_001127511.2:c.7971C= NP_001120983.2:p.Pro2657=
NM_001354895.1:c.8025C= NP_001341824.1:p.Pro2675=
NM_001354896.1:c.8079C= NP_001341825.1:p.Pro2693=
NM_001354897.1:c.8055C= NP_001341826.1:p.Pro2685=
NM_001354898.1:c.7950C= NP_001341827.1:p.Pro2650=
NM_001354899.1:c.7941C= NP_001341828.1:p.Pro2647=
NM_001354900.1:c.7902C= NP_001341829.1:p.Pro2634=
NM_001354901.1:c.7848C= NP_001341830.1:p.Pro2616=
NM_001354902.1:c.7752C= NP_001341831.1:p.Pro2584=
NM_001354903.1:c.7722C= NP_001341832.1:p.Pro2574=
NM_001354904.1:c.7647C= NP_001341833.1:p.Pro2549=
NM_001354905.1:c.7545C= NP_001341834.1:p.Pro2515=
NM_001354906.1:c.7176C= NP_001341835.1:p.Pro2392=
NM_000038.6:c.8025C= MANE Select NP_000029.2:p.Pro2675=
NM_001127510.3:c.8025C= NP_001120982.1:p.Pro2675=
NM_001127511.3:c.7971C= NP_001120983.2:p.Pro2657=
NM_001354895.2:c.8025C= NP_001341824.1:p.Pro2675=
NM_001354896.2:c.8079C= NP_001341825.1:p.Pro2693=
NM_001354897.2:c.8055C= NP_001341826.1:p.Pro2685=
NM_001354898.2:c.7950C= NP_001341827.1:p.Pro2650=
NM_001354899.2:c.7941C= NP_001341828.1:p.Pro2647=
NM_001354900.2:c.7902C= NP_001341829.1:p.Pro2634=
NM_001354901.2:c.7848C= NP_001341830.1:p.Pro2616=
NM_001354902.2:c.7752C= NP_001341831.1:p.Pro2584=
NM_001354903.2:c.7722C= NP_001341832.1:p.Pro2574=
NM_001354904.2:c.7647C= NP_001341833.1:p.Pro2549=
NM_001354905.2:c.7545C= NP_001341834.1:p.Pro2515=
NM_001354906.2:c.7176C= NP_001341835.1:p.Pro2392=