Canonical Allele Identifier: CA011556
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 82456
ClinVar RCV Id: RCV000073445
dbSNP Id: rs74873706

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112786037C>A , CM000667.2:g.112786037C>A GRCh38
NC_000005.9:g.112121734C>A , CM000667.1:g.112121734C>A GRCh37
NC_000005.8:g.112149633C>A NCBI36
NG_008481.4:g.98517C>A , LRG_130:g.98517C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000502371.3:c.645+5134C>A ENSP00000484935.2:n.645+5134C>A
ENST00000504915.3:c.645+5134C>A ENSP00000473355.2:n.645+5134C>A
ENST00000505084.2:n.701+5134C>A
ENST00000505350.2:c.*651+5134C>A ENSP00000481752.1:n.*651+5134C>A
ENST00000507379.6:c.675+5134C>A ENSP00000423224.2:n.675+5134C>A
ENST00000509732.6:c.645+5134C>A ENSP00000426541.2:n.645+5134C>A
ENST00000512211.7:c.645+5134C>A ENSP00000423828.3:n.645+5134C>A
ENST00000257430.9:c.645+5134C>A MANE Select ENSP00000257430.4:n.645+5134C>A
ENST00000257430.8:c.645+5134C>A ENSP00000257430.4:n.645+5134C>A
ENST00000507379.5:c.675+5134C>A ENSP00000423224.1:n.675+5134C>A
ENST00000508376.6:c.645+5134C>A ENSP00000427089.2:n.645+5134C>A
ENST00000508624.5:c.645+5134C>A ENSP00000424265.1:n.645+5134C>A
ENST00000512211.6:c.645+5134C>A ENSP00000423828.2:n.645+5134C>A
NM_000038.5:c.645+5134C>A NP_000029.2:n.645+5134C>A
NM_001127510.2:c.645+5134C>A NP_001120982.1:n.645+5134C>A
NM_001127511.2:c.675+5134C>A NP_001120983.2:n.675+5134C>A
NM_001354895.1:c.645+5134C>A NP_001341824.1:n.645+5134C>A
NM_001354896.1:c.645+5134C>A NP_001341825.1:n.645+5134C>A
NM_001354897.1:c.675+5134C>A NP_001341826.1:n.675+5134C>A
NM_001354898.1:c.570+5134C>A NP_001341827.1:n.570+5134C>A
NM_001354899.1:c.645+5134C>A NP_001341828.1:n.645+5134C>A
NM_001354900.1:c.468+5134C>A NP_001341829.1:n.468+5134C>A
NM_001354901.1:c.468+5134C>A NP_001341830.1:n.468+5134C>A
NM_001354902.1:c.675+5134C>A NP_001341831.1:n.675+5134C>A
NM_001354903.1:c.645+5134C>A NP_001341832.1:n.645+5134C>A
NM_001354904.1:c.570+5134C>A NP_001341833.1:n.570+5134C>A
NM_001354905.1:c.468+5134C>A NP_001341834.1:n.468+5134C>A
NM_001354906.1:c.-391+5134C>A NP_001341835.1:n.-391+5134C>A
NM_000038.6:c.645+5134C>A MANE Select NP_000029.2:n.645+5134C>A
NM_001127510.3:c.645+5134C>A NP_001120982.1:n.645+5134C>A
NM_001127511.3:c.675+5134C>A NP_001120983.2:n.675+5134C>A
NM_001354895.2:c.645+5134C>A NP_001341824.1:n.645+5134C>A
NM_001354896.2:c.645+5134C>A NP_001341825.1:n.645+5134C>A
NM_001354897.2:c.675+5134C>A NP_001341826.1:n.675+5134C>A
NM_001354898.2:c.570+5134C>A NP_001341827.1:n.570+5134C>A
NM_001354899.2:c.645+5134C>A NP_001341828.1:n.645+5134C>A
NM_001354900.2:c.468+5134C>A NP_001341829.1:n.468+5134C>A
NM_001354901.2:c.468+5134C>A NP_001341830.1:n.468+5134C>A
NM_001354902.2:c.675+5134C>A NP_001341831.1:n.675+5134C>A
NM_001354903.2:c.645+5134C>A NP_001341832.1:n.645+5134C>A
NM_001354904.2:c.570+5134C>A NP_001341833.1:n.570+5134C>A
NM_001354905.2:c.468+5134C>A NP_001341834.1:n.468+5134C>A
NM_001354906.2:c.-391+5134C>A NP_001341835.1:n.-391+5134C>A