Canonical Allele Identifier: CA445758946
Gene: APC HGNC NCBI

Linked Data

dbSNP Id: rs2149844344
MyVariant Identifiers: chr5:g.112170848A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112835151A>G , CM000667.2:g.112835151A>G GRCh38
NC_000005.9:g.112170848A>G , CM000667.1:g.112170848A>G GRCh37
NC_000005.8:g.112198747A>G NCBI36
NG_008481.4:g.147631A>G , LRG_130:g.147631A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000502371.3:c.1609A>G ENSP00000484935.2:n.1609A>G
ENST00000504915.3:c.1998A>G ENSP00000473355.2:p.Thr666=
ENST00000505350.2:c.*1950A>G ENSP00000481752.1:n.*1950A>G
ENST00000507379.6:c.1890A>G ENSP00000423224.2:p.Thr630=
ENST00000509732.6:c.1944A>G ENSP00000426541.2:p.Thr648=
ENST00000512211.7:c.1944A>G ENSP00000423828.3:p.Thr648=
ENST00000257430.9:c.1944A>G MANE Select ENSP00000257430.4:p.Thr648=
ENST00000257430.8:c.1944A>G ENSP00000257430.4:p.Thr648=
ENST00000502371.2:c.297A>G
ENST00000504915.2:c.633A>G ENSP00000473355.1:p.Thr211=
ENST00000507379.5:c.1890A>G ENSP00000423224.1:p.Thr630=
ENST00000508376.6:c.1944A>G ENSP00000427089.2:p.Thr648=
ENST00000508624.5:c.*1266A>G ENSP00000424265.1:n.*1266A>G
ENST00000512211.6:c.1944A>G ENSP00000423828.2:p.Thr648=
ENST00000520401.1:c.230+6179A>G
NM_000038.5:c.1944A>G NP_000029.2:p.Thr648=
NM_001127510.2:c.1944A>G NP_001120982.1:p.Thr648=
NM_001127511.2:c.1890A>G NP_001120983.2:p.Thr630=
NM_001354895.1:c.1944A>G NP_001341824.1:p.Thr648=
NM_001354896.1:c.1998A>G NP_001341825.1:p.Thr666=
NM_001354897.1:c.1974A>G NP_001341826.1:p.Thr658=
NM_001354898.1:c.1869A>G NP_001341827.1:p.Thr623=
NM_001354899.1:c.1860A>G NP_001341828.1:p.Thr620=
NM_001354900.1:c.1821A>G NP_001341829.1:p.Thr607=
NM_001354901.1:c.1767A>G NP_001341830.1:p.Thr589=
NM_001354902.1:c.1671A>G NP_001341831.1:p.Thr557=
NM_001354903.1:c.1641A>G NP_001341832.1:p.Thr547=
NM_001354904.1:c.1566A>G NP_001341833.1:p.Thr522=
NM_001354905.1:c.1464A>G NP_001341834.1:p.Thr488=
NM_001354906.1:c.1095A>G NP_001341835.1:p.Thr365=
NM_000038.6:c.1944A>G MANE Select NP_000029.2:p.Thr648=
NM_001127510.3:c.1944A>G NP_001120982.1:p.Thr648=
NM_001127511.3:c.1890A>G NP_001120983.2:p.Thr630=
NM_001354895.2:c.1944A>G NP_001341824.1:p.Thr648=
NM_001354896.2:c.1998A>G NP_001341825.1:p.Thr666=
NM_001354897.2:c.1974A>G NP_001341826.1:p.Thr658=
NM_001354898.2:c.1869A>G NP_001341827.1:p.Thr623=
NM_001354899.2:c.1860A>G NP_001341828.1:p.Thr620=
NM_001354900.2:c.1821A>G NP_001341829.1:p.Thr607=
NM_001354901.2:c.1767A>G NP_001341830.1:p.Thr589=
NM_001354902.2:c.1671A>G NP_001341831.1:p.Thr557=
NM_001354903.2:c.1641A>G NP_001341832.1:p.Thr547=
NM_001354904.2:c.1566A>G NP_001341833.1:p.Thr522=
NM_001354905.2:c.1464A>G NP_001341834.1:p.Thr488=
NM_001354906.2:c.1095A>G NP_001341835.1:p.Thr365=