Canonical Allele Identifier: CA16028455
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112838841G>C , CM000667.2:g.112838841G>C GRCh38
NC_000005.9:g.112174538G>C , CM000667.1:g.112174538G>C GRCh37
NC_000005.8:g.112202437G>C NCBI36
NG_008481.4:g.151321G>C , LRG_130:g.151321G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000502371.3:c.2912G>C ENSP00000484935.2:n.2912G>C
ENST00000504915.3:c.3301G>C ENSP00000473355.2:p.Asp1101His
ENST00000505350.2:c.*3253G>C ENSP00000481752.1:n.*3253G>C
ENST00000507379.6:c.3193G>C ENSP00000423224.2:p.Asp1065His
ENST00000509732.6:c.3247G>C ENSP00000426541.2:p.Asp1083His
ENST00000512211.7:c.3247G>C ENSP00000423828.3:p.Asp1083His
ENST00000257430.9:c.3247G>C MANE Select ENSP00000257430.4:p.Asp1083His
ENST00000257430.8:c.3247G>C ENSP00000257430.4:p.Asp1083His
ENST00000502371.2:c.1600G>C
ENST00000507379.5:c.3193G>C ENSP00000423224.1:p.Asp1065His
ENST00000508376.6:c.3247G>C ENSP00000427089.2:p.Asp1083His
ENST00000508624.5:c.*2569G>C ENSP00000424265.1:n.*2569G>C
ENST00000512211.6:c.3247G>C ENSP00000423828.2:p.Asp1083His
ENST00000520401.1:c.230+9869G>C
NM_000038.5:c.3247G>C NP_000029.2:p.Asp1083His
NM_001127510.2:c.3247G>C NP_001120982.1:p.Asp1083His
NM_001127511.2:c.3193G>C NP_001120983.2:p.Asp1065His
NM_001354895.1:c.3247G>C NP_001341824.1:p.Asp1083His
NM_001354896.1:c.3301G>C NP_001341825.1:p.Asp1101His
NM_001354897.1:c.3277G>C NP_001341826.1:p.Asp1093His
NM_001354898.1:c.3172G>C NP_001341827.1:p.Asp1058His
NM_001354899.1:c.3163G>C NP_001341828.1:p.Asp1055His
NM_001354900.1:c.3124G>C NP_001341829.1:p.Asp1042His
NM_001354901.1:c.3070G>C NP_001341830.1:p.Asp1024His
NM_001354902.1:c.2974G>C NP_001341831.1:p.Asp992His
NM_001354903.1:c.2944G>C NP_001341832.1:p.Asp982His
NM_001354904.1:c.2869G>C NP_001341833.1:p.Asp957His
NM_001354905.1:c.2767G>C NP_001341834.1:p.Asp923His
NM_001354906.1:c.2398G>C NP_001341835.1:p.Asp800His
NM_000038.6:c.3247G>C MANE Select NP_000029.2:p.Asp1083His
NM_001127510.3:c.3247G>C NP_001120982.1:p.Asp1083His
NM_001127511.3:c.3193G>C NP_001120983.2:p.Asp1065His
NM_001354895.2:c.3247G>C NP_001341824.1:p.Asp1083His
NM_001354896.2:c.3301G>C NP_001341825.1:p.Asp1101His
NM_001354897.2:c.3277G>C NP_001341826.1:p.Asp1093His
NM_001354898.2:c.3172G>C NP_001341827.1:p.Asp1058His
NM_001354899.2:c.3163G>C NP_001341828.1:p.Asp1055His
NM_001354900.2:c.3124G>C NP_001341829.1:p.Asp1042His
NM_001354901.2:c.3070G>C NP_001341830.1:p.Asp1024His
NM_001354902.2:c.2974G>C NP_001341831.1:p.Asp992His
NM_001354903.2:c.2944G>C NP_001341832.1:p.Asp982His
NM_001354904.2:c.2869G>C NP_001341833.1:p.Asp957His
NM_001354905.2:c.2767G>C NP_001341834.1:p.Asp923His
NM_001354906.2:c.2398G>C NP_001341835.1:p.Asp800His