Canonical Allele Identifier: CA008967

Gene: APC

Linked Data

• ClinVar Variation Id: 142519
• ClinVar RCV Id: RCV000131673 ; RCV003337237
• dbSNP Id: rs587782518
• COSMIC: COSM19087
• MyVariant Identifiers: chr5:g.112175507C>T (hg19) ; chr5:g.112839810C>T (hg38)
• PubMed: PMID:8187091 ; PMID:12010888 ; PMID:20685668

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112839810C>T , CM000667.2:g.112839810C>T	GRCh38
NC_000005.9:g.112175507C>T , CM000667.1:g.112175507C>T	GRCh37
NC_000005.8:g.112203406C>T	NCBI36
NG_008481.4:g.152290C>T , LRG_130:g.152290C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.3881C>T	ENSP00000484935.2:n.3881C>T
ENST00000504915.3:c.4270C>T	ENSP00000473355.2:p.Gln1424Ter
ENST00000505350.2:c.*4222C>T	ENSP00000481752.1:n.*4222C>T
ENST00000507379.6:c.4162C>T	ENSP00000423224.2:p.Gln1388Ter
ENST00000509732.6:c.4216C>T	ENSP00000426541.2:p.Gln1406Ter
ENST00000512211.7:c.4216C>T	ENSP00000423828.3:p.Gln1406Ter
ENST00000257430.9:c.4216C>T MANE Select	ENSP00000257430.4:p.Gln1406Ter
ENST00000257430.8:c.4216C>T	ENSP00000257430.4:p.Gln1406Ter
ENST00000502371.2:c.2569C>T
ENST00000508376.6:c.4216C>T	ENSP00000427089.2:p.Gln1406Ter
ENST00000508624.5:c.*3538C>T	ENSP00000424265.1:n.*3538C>T
ENST00000520401.1:c.230+10838C>T
NM_000038.5:c.4216C>T	NP_000029.2:p.Gln1406Ter
NM_001127510.2:c.4216C>T	NP_001120982.1:p.Gln1406Ter
NM_001127511.2:c.4162C>T	NP_001120983.2:p.Gln1388Ter
NM_001354895.1:c.4216C>T	NP_001341824.1:p.Gln1406Ter
NM_001354896.1:c.4270C>T	NP_001341825.1:p.Gln1424Ter
NM_001354897.1:c.4246C>T	NP_001341826.1:p.Gln1416Ter
NM_001354898.1:c.4141C>T	NP_001341827.1:p.Gln1381Ter
NM_001354899.1:c.4132C>T	NP_001341828.1:p.Gln1378Ter
NM_001354900.1:c.4093C>T	NP_001341829.1:p.Gln1365Ter
NM_001354901.1:c.4039C>T	NP_001341830.1:p.Gln1347Ter
NM_001354902.1:c.3943C>T	NP_001341831.1:p.Gln1315Ter
NM_001354903.1:c.3913C>T	NP_001341832.1:p.Gln1305Ter
NM_001354904.1:c.3838C>T	NP_001341833.1:p.Gln1280Ter
NM_001354905.1:c.3736C>T	NP_001341834.1:p.Gln1246Ter
NM_001354906.1:c.3367C>T	NP_001341835.1:p.Gln1123Ter
NM_000038.6:c.4216C>T MANE Select	NP_000029.2:p.Gln1406Ter
NM_001127510.3:c.4216C>T	NP_001120982.1:p.Gln1406Ter
NM_001127511.3:c.4162C>T	NP_001120983.2:p.Gln1388Ter
NM_001354895.2:c.4216C>T	NP_001341824.1:p.Gln1406Ter
NM_001354896.2:c.4270C>T	NP_001341825.1:p.Gln1424Ter
NM_001354897.2:c.4246C>T	NP_001341826.1:p.Gln1416Ter
NM_001354898.2:c.4141C>T	NP_001341827.1:p.Gln1381Ter
NM_001354899.2:c.4132C>T	NP_001341828.1:p.Gln1378Ter
NM_001354900.2:c.4093C>T	NP_001341829.1:p.Gln1365Ter
NM_001354901.2:c.4039C>T	NP_001341830.1:p.Gln1347Ter
NM_001354902.2:c.3943C>T	NP_001341831.1:p.Gln1315Ter
NM_001354903.2:c.3913C>T	NP_001341832.1:p.Gln1305Ter
NM_001354904.2:c.3838C>T	NP_001341833.1:p.Gln1280Ter
NM_001354905.2:c.3736C>T	NP_001341834.1:p.Gln1246Ter
NM_001354906.2:c.3367C>T	NP_001341835.1:p.Gln1123Ter