Canonical Allele Identifier: CA16030720

Gene: APC

Linked Data

• ClinVar Variation Id: 376063
• ClinVar RCV Id: RCV000433006 ; RCV003337273
• dbSNP Id: rs74535574
• COSMIC: COSM18836
• MyVariant Identifiers: chr5:g.112175576C>T (hg19) ; chr5:g.112839879C>T (hg38)
• PubMed: PMID:1528264 ; PMID:8187091 ; PMID:10737795 ; PMID:12374230 ; PMID:22810696 ; PMID:22848674 ; PMID:25157968

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112839879C>T , CM000667.2:g.112839879C>T	GRCh38
NC_000005.9:g.112175576C>T , CM000667.1:g.112175576C>T	GRCh37
NC_000005.8:g.112203475C>T	NCBI36
NG_008481.4:g.152359C>T , LRG_130:g.152359C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4339C>T	ENSP00000473355.2:p.Gln1447Ter
ENST00000505350.2:c.*4291C>T	ENSP00000481752.1:n.*4291C>T
ENST00000507379.6:c.4231C>T	ENSP00000423224.2:p.Gln1411Ter
ENST00000509732.6:c.4285C>T	ENSP00000426541.2:p.Gln1429Ter
ENST00000512211.7:c.4285C>T	ENSP00000423828.3:p.Gln1429Ter
ENST00000257430.9:c.4285C>T MANE Select	ENSP00000257430.4:p.Gln1429Ter
ENST00000257430.8:c.4285C>T	ENSP00000257430.4:p.Gln1429Ter
ENST00000508376.6:c.4285C>T	ENSP00000427089.2:p.Gln1429Ter
ENST00000508624.5:c.*3607C>T	ENSP00000424265.1:n.*3607C>T
ENST00000520401.1:c.230+10907C>T
NM_000038.5:c.4285C>T	NP_000029.2:p.Gln1429Ter
NM_001127510.2:c.4285C>T	NP_001120982.1:p.Gln1429Ter
NM_001127511.2:c.4231C>T	NP_001120983.2:p.Gln1411Ter
NM_001354895.1:c.4285C>T	NP_001341824.1:p.Gln1429Ter
NM_001354896.1:c.4339C>T	NP_001341825.1:p.Gln1447Ter
NM_001354897.1:c.4315C>T	NP_001341826.1:p.Gln1439Ter
NM_001354898.1:c.4210C>T	NP_001341827.1:p.Gln1404Ter
NM_001354899.1:c.4201C>T	NP_001341828.1:p.Gln1401Ter
NM_001354900.1:c.4162C>T	NP_001341829.1:p.Gln1388Ter
NM_001354901.1:c.4108C>T	NP_001341830.1:p.Gln1370Ter
NM_001354902.1:c.4012C>T	NP_001341831.1:p.Gln1338Ter
NM_001354903.1:c.3982C>T	NP_001341832.1:p.Gln1328Ter
NM_001354904.1:c.3907C>T	NP_001341833.1:p.Gln1303Ter
NM_001354905.1:c.3805C>T	NP_001341834.1:p.Gln1269Ter
NM_001354906.1:c.3436C>T	NP_001341835.1:p.Gln1146Ter
NM_000038.6:c.4285C>T MANE Select	NP_000029.2:p.Gln1429Ter
NM_001127510.3:c.4285C>T	NP_001120982.1:p.Gln1429Ter
NM_001127511.3:c.4231C>T	NP_001120983.2:p.Gln1411Ter
NM_001354895.2:c.4285C>T	NP_001341824.1:p.Gln1429Ter
NM_001354896.2:c.4339C>T	NP_001341825.1:p.Gln1447Ter
NM_001354897.2:c.4315C>T	NP_001341826.1:p.Gln1439Ter
NM_001354898.2:c.4210C>T	NP_001341827.1:p.Gln1404Ter
NM_001354899.2:c.4201C>T	NP_001341828.1:p.Gln1401Ter
NM_001354900.2:c.4162C>T	NP_001341829.1:p.Gln1388Ter
NM_001354901.2:c.4108C>T	NP_001341830.1:p.Gln1370Ter
NM_001354902.2:c.4012C>T	NP_001341831.1:p.Gln1338Ter
NM_001354903.2:c.3982C>T	NP_001341832.1:p.Gln1328Ter
NM_001354904.2:c.3907C>T	NP_001341833.1:p.Gln1303Ter
NM_001354905.2:c.3805C>T	NP_001341834.1:p.Gln1269Ter
NM_001354906.2:c.3436C>T	NP_001341835.1:p.Gln1146Ter