Canonical Allele Identifier: CA1573475601
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112843628T= , CM000667.2:g.112843628T= GRCh38
NC_000005.9:g.112179325T= , CM000667.1:g.112179325T= GRCh37
NC_000005.8:g.112207224T= NCBI36
NG_008481.4:g.156108T= , LRG_130:g.156108T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000504915.3:c.8088T= ENSP00000473355.2:p.Asn2696=
ENST00000505350.2:c.*8040T= ENSP00000481752.1:n.*8040T=
ENST00000507379.6:c.7980T= ENSP00000423224.2:p.Asn2660=
ENST00000509732.6:c.8034T= ENSP00000426541.2:p.Asn2678=
ENST00000512211.7:c.8034T= ENSP00000423828.3:p.Asn2678=
ENST00000257430.9:c.8034T= MANE Select ENSP00000257430.4:p.Asn2678=
ENST00000257430.8:c.8034T= ENSP00000257430.4:p.Asn2678=
ENST00000508376.6:c.8034T= ENSP00000427089.2:p.Asn2678=
ENST00000520401.1:c.231-13021T=
NM_000038.5:c.8034T= NP_000029.2:p.Asn2678=
NM_001127510.2:c.8034T= NP_001120982.1:p.Asn2678=
NM_001127511.2:c.7980T= NP_001120983.2:p.Asn2660=
NM_001354895.1:c.8034T= NP_001341824.1:p.Asn2678=
NM_001354896.1:c.8088T= NP_001341825.1:p.Asn2696=
NM_001354897.1:c.8064T= NP_001341826.1:p.Asn2688=
NM_001354898.1:c.7959T= NP_001341827.1:p.Asn2653=
NM_001354899.1:c.7950T= NP_001341828.1:p.Asn2650=
NM_001354900.1:c.7911T= NP_001341829.1:p.Asn2637=
NM_001354901.1:c.7857T= NP_001341830.1:p.Asn2619=
NM_001354902.1:c.7761T= NP_001341831.1:p.Asn2587=
NM_001354903.1:c.7731T= NP_001341832.1:p.Asn2577=
NM_001354904.1:c.7656T= NP_001341833.1:p.Asn2552=
NM_001354905.1:c.7554T= NP_001341834.1:p.Asn2518=
NM_001354906.1:c.7185T= NP_001341835.1:p.Asn2395=
NM_000038.6:c.8034T= MANE Select NP_000029.2:p.Asn2678=
NM_001127510.3:c.8034T= NP_001120982.1:p.Asn2678=
NM_001127511.3:c.7980T= NP_001120983.2:p.Asn2660=
NM_001354895.2:c.8034T= NP_001341824.1:p.Asn2678=
NM_001354896.2:c.8088T= NP_001341825.1:p.Asn2696=
NM_001354897.2:c.8064T= NP_001341826.1:p.Asn2688=
NM_001354898.2:c.7959T= NP_001341827.1:p.Asn2653=
NM_001354899.2:c.7950T= NP_001341828.1:p.Asn2650=
NM_001354900.2:c.7911T= NP_001341829.1:p.Asn2637=
NM_001354901.2:c.7857T= NP_001341830.1:p.Asn2619=
NM_001354902.2:c.7761T= NP_001341831.1:p.Asn2587=
NM_001354903.2:c.7731T= NP_001341832.1:p.Asn2577=
NM_001354904.2:c.7656T= NP_001341833.1:p.Asn2552=
NM_001354905.2:c.7554T= NP_001341834.1:p.Asn2518=
NM_001354906.2:c.7185T= NP_001341835.1:p.Asn2395=