Canonical Allele Identifier: CA1573471034
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112840302G= , CM000667.2:g.112840302G= GRCh38
NC_000005.9:g.112175999G= , CM000667.1:g.112175999G= GRCh37
NC_000005.8:g.112203898G= NCBI36
NG_008481.4:g.152782G= , LRG_130:g.152782G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000504915.3:c.4762G= ENSP00000473355.2:p.Asp1588=
ENST00000505350.2:c.*4714G= ENSP00000481752.1:n.*4714G=
ENST00000507379.6:c.4654G= ENSP00000423224.2:p.Asp1552=
ENST00000509732.6:c.4708G= ENSP00000426541.2:p.Asp1570=
ENST00000512211.7:c.4708G= ENSP00000423828.3:p.Asp1570=
ENST00000257430.9:c.4708G= MANE Select ENSP00000257430.4:p.Asp1570=
ENST00000257430.8:c.4708G= ENSP00000257430.4:p.Asp1570=
ENST00000508376.6:c.4708G= ENSP00000427089.2:p.Asp1570=
ENST00000508624.5:c.*4030G= ENSP00000424265.1:n.*4030G=
ENST00000520401.1:c.230+11330G=
NM_000038.5:c.4708G= NP_000029.2:p.Asp1570=
NM_001127510.2:c.4708G= NP_001120982.1:p.Asp1570=
NM_001127511.2:c.4654G= NP_001120983.2:p.Asp1552=
NM_001354895.1:c.4708G= NP_001341824.1:p.Asp1570=
NM_001354896.1:c.4762G= NP_001341825.1:p.Asp1588=
NM_001354897.1:c.4738G= NP_001341826.1:p.Asp1580=
NM_001354898.1:c.4633G= NP_001341827.1:p.Asp1545=
NM_001354899.1:c.4624G= NP_001341828.1:p.Asp1542=
NM_001354900.1:c.4585G= NP_001341829.1:p.Asp1529=
NM_001354901.1:c.4531G= NP_001341830.1:p.Asp1511=
NM_001354902.1:c.4435G= NP_001341831.1:p.Asp1479=
NM_001354903.1:c.4405G= NP_001341832.1:p.Asp1469=
NM_001354904.1:c.4330G= NP_001341833.1:p.Asp1444=
NM_001354905.1:c.4228G= NP_001341834.1:p.Asp1410=
NM_001354906.1:c.3859G= NP_001341835.1:p.Asp1287=
NM_000038.6:c.4708G= MANE Select NP_000029.2:p.Asp1570=
NM_001127510.3:c.4708G= NP_001120982.1:p.Asp1570=
NM_001127511.3:c.4654G= NP_001120983.2:p.Asp1552=
NM_001354895.2:c.4708G= NP_001341824.1:p.Asp1570=
NM_001354896.2:c.4762G= NP_001341825.1:p.Asp1588=
NM_001354897.2:c.4738G= NP_001341826.1:p.Asp1580=
NM_001354898.2:c.4633G= NP_001341827.1:p.Asp1545=
NM_001354899.2:c.4624G= NP_001341828.1:p.Asp1542=
NM_001354900.2:c.4585G= NP_001341829.1:p.Asp1529=
NM_001354901.2:c.4531G= NP_001341830.1:p.Asp1511=
NM_001354902.2:c.4435G= NP_001341831.1:p.Asp1479=
NM_001354903.2:c.4405G= NP_001341832.1:p.Asp1469=
NM_001354904.2:c.4330G= NP_001341833.1:p.Asp1444=
NM_001354905.2:c.4228G= NP_001341834.1:p.Asp1410=
NM_001354906.2:c.3859G= NP_001341835.1:p.Asp1287=