Canonical Allele Identifier: CA1573471308
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112840348C= , CM000667.2:g.112840348C= GRCh38
NC_000005.9:g.112176045C= , CM000667.1:g.112176045C= GRCh37
NC_000005.8:g.112203944C= NCBI36
NG_008481.4:g.152828C= , LRG_130:g.152828C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000504915.3:c.4808C= ENSP00000473355.2:p.Thr1603=
ENST00000505350.2:c.*4760C= ENSP00000481752.1:n.*4760C=
ENST00000507379.6:c.4700C= ENSP00000423224.2:p.Thr1567=
ENST00000509732.6:c.4754C= ENSP00000426541.2:p.Thr1585=
ENST00000512211.7:c.4754C= ENSP00000423828.3:p.Thr1585=
ENST00000257430.9:c.4754C= MANE Select ENSP00000257430.4:p.Thr1585=
ENST00000257430.8:c.4754C= ENSP00000257430.4:p.Thr1585=
ENST00000508376.6:c.4754C= ENSP00000427089.2:p.Thr1585=
ENST00000508624.5:c.*4076C= ENSP00000424265.1:n.*4076C=
ENST00000520401.1:c.230+11376C=
NM_000038.5:c.4754C= NP_000029.2:p.Thr1585=
NM_001127510.2:c.4754C= NP_001120982.1:p.Thr1585=
NM_001127511.2:c.4700C= NP_001120983.2:p.Thr1567=
NM_001354895.1:c.4754C= NP_001341824.1:p.Thr1585=
NM_001354896.1:c.4808C= NP_001341825.1:p.Thr1603=
NM_001354897.1:c.4784C= NP_001341826.1:p.Thr1595=
NM_001354898.1:c.4679C= NP_001341827.1:p.Thr1560=
NM_001354899.1:c.4670C= NP_001341828.1:p.Thr1557=
NM_001354900.1:c.4631C= NP_001341829.1:p.Thr1544=
NM_001354901.1:c.4577C= NP_001341830.1:p.Thr1526=
NM_001354902.1:c.4481C= NP_001341831.1:p.Thr1494=
NM_001354903.1:c.4451C= NP_001341832.1:p.Thr1484=
NM_001354904.1:c.4376C= NP_001341833.1:p.Thr1459=
NM_001354905.1:c.4274C= NP_001341834.1:p.Thr1425=
NM_001354906.1:c.3905C= NP_001341835.1:p.Thr1302=
NM_000038.6:c.4754C= MANE Select NP_000029.2:p.Thr1585=
NM_001127510.3:c.4754C= NP_001120982.1:p.Thr1585=
NM_001127511.3:c.4700C= NP_001120983.2:p.Thr1567=
NM_001354895.2:c.4754C= NP_001341824.1:p.Thr1585=
NM_001354896.2:c.4808C= NP_001341825.1:p.Thr1603=
NM_001354897.2:c.4784C= NP_001341826.1:p.Thr1595=
NM_001354898.2:c.4679C= NP_001341827.1:p.Thr1560=
NM_001354899.2:c.4670C= NP_001341828.1:p.Thr1557=
NM_001354900.2:c.4631C= NP_001341829.1:p.Thr1544=
NM_001354901.2:c.4577C= NP_001341830.1:p.Thr1526=
NM_001354902.2:c.4481C= NP_001341831.1:p.Thr1494=
NM_001354903.2:c.4451C= NP_001341832.1:p.Thr1484=
NM_001354904.2:c.4376C= NP_001341833.1:p.Thr1459=
NM_001354905.2:c.4274C= NP_001341834.1:p.Thr1425=
NM_001354906.2:c.3905C= NP_001341835.1:p.Thr1302=