Canonical Allele Identifier: CA2709972467
Gene: APC HGNC NCBI

Linked Data

dbSNP Id: rs2149787189

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112767149_112767150del , CM000667.2:g.112767149_112767150del GRCh38
NC_000005.9:g.112102846_112102847del , CM000667.1:g.112102846_112102847del GRCh37
NC_000005.8:g.112130745_112130746del NCBI36
NG_008481.4:g.79629_79630del , LRG_130:g.79629_79630del

Transcript Alleles

HGVS Amino-acid change
ENST00000502371.3:c.221-40_221-39del ENSP00000484935.2:n.221-40_221-39del
ENST00000504915.3:c.221-40_221-39del ENSP00000473355.2:n.221-40_221-39del
ENST00000505084.2:n.277-40_277-39del
ENST00000505350.2:c.*227-40_*227-39del ENSP00000481752.1:n.*227-40_*227-39del
ENST00000507379.6:c.251-40_251-39del ENSP00000423224.2:n.251-40_251-39del
ENST00000509732.6:c.221-40_221-39del ENSP00000426541.2:n.221-40_221-39del
ENST00000512211.7:c.221-40_221-39del ENSP00000423828.3:n.221-40_221-39del
ENST00000257430.9:c.221-40_221-39del MANE Select ENSP00000257430.4:n.221-40_221-39del
ENST00000257430.8:c.221-40_221-39del ENSP00000257430.4:n.221-40_221-39del
ENST00000507379.5:c.251-40_251-39del ENSP00000423224.1:n.251-40_251-39del
ENST00000508376.6:c.221-40_221-39del ENSP00000427089.2:n.221-40_221-39del
ENST00000508624.5:c.221-40_221-39del ENSP00000424265.1:n.221-40_221-39del
ENST00000509732.5:c.221-40_221-39del ENSP00000426541.1:n.221-40_221-39del
ENST00000512211.6:c.221-40_221-39del ENSP00000423828.2:n.221-40_221-39del
NM_000038.5:c.221-40_221-39del NP_000029.2:n.221-40_221-39del
NM_001127510.2:c.221-40_221-39del NP_001120982.1:n.221-40_221-39del
NM_001127511.2:c.251-40_251-39del NP_001120983.2:n.251-40_251-39del
NM_001354895.1:c.221-40_221-39del NP_001341824.1:n.221-40_221-39del
NM_001354896.1:c.221-40_221-39del NP_001341825.1:n.221-40_221-39del
NM_001354897.1:c.251-40_251-39del NP_001341826.1:n.251-40_251-39del
NM_001354898.1:c.146-40_146-39del NP_001341827.1:n.146-40_146-39del
NM_001354899.1:c.221-40_221-39del NP_001341828.1:n.221-40_221-39del
NM_001354900.1:c.44-40_44-39del NP_001341829.1:n.44-40_44-39del
NM_001354901.1:c.44-40_44-39del NP_001341830.1:n.44-40_44-39del
NM_001354902.1:c.251-40_251-39del NP_001341831.1:n.251-40_251-39del
NM_001354903.1:c.221-40_221-39del NP_001341832.1:n.221-40_221-39del
NM_001354904.1:c.146-40_146-39del NP_001341833.1:n.146-40_146-39del
NM_001354905.1:c.44-40_44-39del NP_001341834.1:n.44-40_44-39del
NM_001354906.1:c.-815-40_-815-39del NP_001341835.1:n.-815-40_-815-39del
NM_000038.6:c.221-40_221-39del MANE Select NP_000029.2:n.221-40_221-39del
NM_001127510.3:c.221-40_221-39del NP_001120982.1:n.221-40_221-39del
NM_001127511.3:c.251-40_251-39del NP_001120983.2:n.251-40_251-39del
NM_001354895.2:c.221-40_221-39del NP_001341824.1:n.221-40_221-39del
NM_001354896.2:c.221-40_221-39del NP_001341825.1:n.221-40_221-39del
NM_001354897.2:c.251-40_251-39del NP_001341826.1:n.251-40_251-39del
NM_001354898.2:c.146-40_146-39del NP_001341827.1:n.146-40_146-39del
NM_001354899.2:c.221-40_221-39del NP_001341828.1:n.221-40_221-39del
NM_001354900.2:c.44-40_44-39del NP_001341829.1:n.44-40_44-39del
NM_001354901.2:c.44-40_44-39del NP_001341830.1:n.44-40_44-39del
NM_001354902.2:c.251-40_251-39del NP_001341831.1:n.251-40_251-39del
NM_001354903.2:c.221-40_221-39del NP_001341832.1:n.221-40_221-39del
NM_001354904.2:c.146-40_146-39del NP_001341833.1:n.146-40_146-39del
NM_001354905.2:c.44-40_44-39del NP_001341834.1:n.44-40_44-39del
NM_001354906.2:c.-815-40_-815-39del NP_001341835.1:n.-815-40_-815-39del