Canonical Allele Identifier: CA007819
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 136408
dbSNP Id: rs137854575

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112838399C>T , CM000667.2:g.112838399C>T GRCh38
NC_000005.9:g.112174096C>T , CM000667.1:g.112174096C>T GRCh37
NC_000005.8:g.112201995C>T NCBI36
NG_008481.4:g.150879C>T , LRG_130:g.150879C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000502371.3:c.2470C>T ENSP00000484935.2:n.2470C>T
ENST00000504915.3:c.2859C>T ENSP00000473355.2:p.Tyr953=
ENST00000505350.2:c.*2811C>T ENSP00000481752.1:n.*2811C>T
ENST00000507379.6:c.2751C>T ENSP00000423224.2:p.Tyr917=
ENST00000509732.6:c.2805C>T ENSP00000426541.2:p.Tyr935=
ENST00000512211.7:c.2805C>T ENSP00000423828.3:p.Tyr935=
ENST00000257430.9:c.2805C>T MANE Select ENSP00000257430.4:p.Tyr935=
ENST00000257430.8:c.2805C>T ENSP00000257430.4:p.Tyr935=
ENST00000502371.2:c.1158C>T
ENST00000507379.5:c.2751C>T ENSP00000423224.1:p.Tyr917=
ENST00000508376.6:c.2805C>T ENSP00000427089.2:p.Tyr935=
ENST00000508624.5:c.*2127C>T ENSP00000424265.1:n.*2127C>T
ENST00000512211.6:c.2805C>T ENSP00000423828.2:p.Tyr935=
ENST00000520401.1:c.230+9427C>T
NM_000038.5:c.2805C>T NP_000029.2:p.Tyr935=
NM_001127510.2:c.2805C>T NP_001120982.1:p.Tyr935=
NM_001127511.2:c.2751C>T NP_001120983.2:p.Tyr917=
NM_001354895.1:c.2805C>T NP_001341824.1:p.Tyr935=
NM_001354896.1:c.2859C>T NP_001341825.1:p.Tyr953=
NM_001354897.1:c.2835C>T NP_001341826.1:p.Tyr945=
NM_001354898.1:c.2730C>T NP_001341827.1:p.Tyr910=
NM_001354899.1:c.2721C>T NP_001341828.1:p.Tyr907=
NM_001354900.1:c.2682C>T NP_001341829.1:p.Tyr894=
NM_001354901.1:c.2628C>T NP_001341830.1:p.Tyr876=
NM_001354902.1:c.2532C>T NP_001341831.1:p.Tyr844=
NM_001354903.1:c.2502C>T NP_001341832.1:p.Tyr834=
NM_001354904.1:c.2427C>T NP_001341833.1:p.Tyr809=
NM_001354905.1:c.2325C>T NP_001341834.1:p.Tyr775=
NM_001354906.1:c.1956C>T NP_001341835.1:p.Tyr652=
NM_000038.6:c.2805C>T MANE Select NP_000029.2:p.Tyr935=
NM_001127510.3:c.2805C>T NP_001120982.1:p.Tyr935=
NM_001127511.3:c.2751C>T NP_001120983.2:p.Tyr917=
NM_001354895.2:c.2805C>T NP_001341824.1:p.Tyr935=
NM_001354896.2:c.2859C>T NP_001341825.1:p.Tyr953=
NM_001354897.2:c.2835C>T NP_001341826.1:p.Tyr945=
NM_001354898.2:c.2730C>T NP_001341827.1:p.Tyr910=
NM_001354899.2:c.2721C>T NP_001341828.1:p.Tyr907=
NM_001354900.2:c.2682C>T NP_001341829.1:p.Tyr894=
NM_001354901.2:c.2628C>T NP_001341830.1:p.Tyr876=
NM_001354902.2:c.2532C>T NP_001341831.1:p.Tyr844=
NM_001354903.2:c.2502C>T NP_001341832.1:p.Tyr834=
NM_001354904.2:c.2427C>T NP_001341833.1:p.Tyr809=
NM_001354905.2:c.2325C>T NP_001341834.1:p.Tyr775=
NM_001354906.2:c.1956C>T NP_001341835.1:p.Tyr652=