Canonical Allele Identifier: CA1573475627
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112843632C= , CM000667.2:g.112843632C= GRCh38
NC_000005.9:g.112179329C= , CM000667.1:g.112179329C= GRCh37
NC_000005.8:g.112207228C= NCBI36
NG_008481.4:g.156112C= , LRG_130:g.156112C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000504915.3:c.8092C= ENSP00000473355.2:p.Pro2698=
ENST00000505350.2:c.*8044C= ENSP00000481752.1:n.*8044C=
ENST00000507379.6:c.7984C= ENSP00000423224.2:p.Pro2662=
ENST00000509732.6:c.8038C= ENSP00000426541.2:p.Pro2680=
ENST00000512211.7:c.8038C= ENSP00000423828.3:p.Pro2680=
ENST00000257430.9:c.8038C= MANE Select ENSP00000257430.4:p.Pro2680=
ENST00000257430.8:c.8038C= ENSP00000257430.4:p.Pro2680=
ENST00000508376.6:c.8038C= ENSP00000427089.2:p.Pro2680=
ENST00000520401.1:c.231-13017C=
NM_000038.5:c.8038C= NP_000029.2:p.Pro2680=
NM_001127510.2:c.8038C= NP_001120982.1:p.Pro2680=
NM_001127511.2:c.7984C= NP_001120983.2:p.Pro2662=
NM_001354895.1:c.8038C= NP_001341824.1:p.Pro2680=
NM_001354896.1:c.8092C= NP_001341825.1:p.Pro2698=
NM_001354897.1:c.8068C= NP_001341826.1:p.Pro2690=
NM_001354898.1:c.7963C= NP_001341827.1:p.Pro2655=
NM_001354899.1:c.7954C= NP_001341828.1:p.Pro2652=
NM_001354900.1:c.7915C= NP_001341829.1:p.Pro2639=
NM_001354901.1:c.7861C= NP_001341830.1:p.Pro2621=
NM_001354902.1:c.7765C= NP_001341831.1:p.Pro2589=
NM_001354903.1:c.7735C= NP_001341832.1:p.Pro2579=
NM_001354904.1:c.7660C= NP_001341833.1:p.Pro2554=
NM_001354905.1:c.7558C= NP_001341834.1:p.Pro2520=
NM_001354906.1:c.7189C= NP_001341835.1:p.Pro2397=
NM_000038.6:c.8038C= MANE Select NP_000029.2:p.Pro2680=
NM_001127510.3:c.8038C= NP_001120982.1:p.Pro2680=
NM_001127511.3:c.7984C= NP_001120983.2:p.Pro2662=
NM_001354895.2:c.8038C= NP_001341824.1:p.Pro2680=
NM_001354896.2:c.8092C= NP_001341825.1:p.Pro2698=
NM_001354897.2:c.8068C= NP_001341826.1:p.Pro2690=
NM_001354898.2:c.7963C= NP_001341827.1:p.Pro2655=
NM_001354899.2:c.7954C= NP_001341828.1:p.Pro2652=
NM_001354900.2:c.7915C= NP_001341829.1:p.Pro2639=
NM_001354901.2:c.7861C= NP_001341830.1:p.Pro2621=
NM_001354902.2:c.7765C= NP_001341831.1:p.Pro2589=
NM_001354903.2:c.7735C= NP_001341832.1:p.Pro2579=
NM_001354904.2:c.7660C= NP_001341833.1:p.Pro2554=
NM_001354905.2:c.7558C= NP_001341834.1:p.Pro2520=
NM_001354906.2:c.7189C= NP_001341835.1:p.Pro2397=