Canonical Allele Identifier: CA446210981
Gene: APC HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.112179247T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112843550T>A , CM000667.2:g.112843550T>A GRCh38
NC_000005.9:g.112179247T>A , CM000667.1:g.112179247T>A GRCh37
NC_000005.8:g.112207146T>A NCBI36
NG_008481.4:g.156030T>A , LRG_130:g.156030T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000504915.3:c.8010T>A ENSP00000473355.2:p.Ser2670=
ENST00000505350.2:c.*7962T>A ENSP00000481752.1:n.*7962T>A
ENST00000507379.6:c.7902T>A ENSP00000423224.2:p.Ser2634=
ENST00000509732.6:c.7956T>A ENSP00000426541.2:p.Ser2652=
ENST00000512211.7:c.7956T>A ENSP00000423828.3:p.Ser2652=
ENST00000257430.9:c.7956T>A MANE Select ENSP00000257430.4:p.Ser2652=
ENST00000257430.8:c.7956T>A ENSP00000257430.4:p.Ser2652=
ENST00000508376.6:c.7956T>A ENSP00000427089.2:p.Ser2652=
ENST00000520401.1:c.231-13099T>A
NM_000038.5:c.7956T>A NP_000029.2:p.Ser2652=
NM_001127510.2:c.7956T>A NP_001120982.1:p.Ser2652=
NM_001127511.2:c.7902T>A NP_001120983.2:p.Ser2634=
NM_001354895.1:c.7956T>A NP_001341824.1:p.Ser2652=
NM_001354896.1:c.8010T>A NP_001341825.1:p.Ser2670=
NM_001354897.1:c.7986T>A NP_001341826.1:p.Ser2662=
NM_001354898.1:c.7881T>A NP_001341827.1:p.Ser2627=
NM_001354899.1:c.7872T>A NP_001341828.1:p.Ser2624=
NM_001354900.1:c.7833T>A NP_001341829.1:p.Ser2611=
NM_001354901.1:c.7779T>A NP_001341830.1:p.Ser2593=
NM_001354902.1:c.7683T>A NP_001341831.1:p.Ser2561=
NM_001354903.1:c.7653T>A NP_001341832.1:p.Ser2551=
NM_001354904.1:c.7578T>A NP_001341833.1:p.Ser2526=
NM_001354905.1:c.7476T>A NP_001341834.1:p.Ser2492=
NM_001354906.1:c.7107T>A NP_001341835.1:p.Ser2369=
NM_000038.6:c.7956T>A MANE Select NP_000029.2:p.Ser2652=
NM_001127510.3:c.7956T>A NP_001120982.1:p.Ser2652=
NM_001127511.3:c.7902T>A NP_001120983.2:p.Ser2634=
NM_001354895.2:c.7956T>A NP_001341824.1:p.Ser2652=
NM_001354896.2:c.8010T>A NP_001341825.1:p.Ser2670=
NM_001354897.2:c.7986T>A NP_001341826.1:p.Ser2662=
NM_001354898.2:c.7881T>A NP_001341827.1:p.Ser2627=
NM_001354899.2:c.7872T>A NP_001341828.1:p.Ser2624=
NM_001354900.2:c.7833T>A NP_001341829.1:p.Ser2611=
NM_001354901.2:c.7779T>A NP_001341830.1:p.Ser2593=
NM_001354902.2:c.7683T>A NP_001341831.1:p.Ser2561=
NM_001354903.2:c.7653T>A NP_001341832.1:p.Ser2551=
NM_001354904.2:c.7578T>A NP_001341833.1:p.Ser2526=
NM_001354905.2:c.7476T>A NP_001341834.1:p.Ser2492=
NM_001354906.2:c.7107T>A NP_001341835.1:p.Ser2369=