Canonical Allele Identifier: CA16037722

Gene: APC

Linked Data

• ClinVar Variation Id: 1485763
• ClinVar RCV Id: RCV003745494
• dbSNP Id: rs747833393
• MyVariant Identifiers: chr5:g.112178832C>A (hg19) ; chr5:g.112843135C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843135C>A , CM000667.2:g.112843135C>A	GRCh38
NC_000005.9:g.112178832C>A , CM000667.1:g.112178832C>A	GRCh37
NC_000005.8:g.112206731C>A	NCBI36
NG_008481.4:g.155615C>A , LRG_130:g.155615C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7595C>A	ENSP00000473355.2:p.Thr2532Asn
ENST00000505350.2:c.*7547C>A	ENSP00000481752.1:n.*7547C>A
ENST00000507379.6:c.7487C>A	ENSP00000423224.2:p.Thr2496Asn
ENST00000509732.6:c.7541C>A	ENSP00000426541.2:p.Thr2514Asn
ENST00000512211.7:c.7541C>A	ENSP00000423828.3:p.Thr2514Asn
ENST00000257430.9:c.7541C>A MANE Select	ENSP00000257430.4:p.Thr2514Asn
ENST00000257430.8:c.7541C>A	ENSP00000257430.4:p.Thr2514Asn
ENST00000508376.6:c.7541C>A	ENSP00000427089.2:p.Thr2514Asn
ENST00000520401.1:c.231-13514C>A
NM_000038.5:c.7541C>A	NP_000029.2:p.Thr2514Asn
NM_001127510.2:c.7541C>A	NP_001120982.1:p.Thr2514Asn
NM_001127511.2:c.7487C>A	NP_001120983.2:p.Thr2496Asn
NM_001354895.1:c.7541C>A	NP_001341824.1:p.Thr2514Asn
NM_001354896.1:c.7595C>A	NP_001341825.1:p.Thr2532Asn
NM_001354897.1:c.7571C>A	NP_001341826.1:p.Thr2524Asn
NM_001354898.1:c.7466C>A	NP_001341827.1:p.Thr2489Asn
NM_001354899.1:c.7457C>A	NP_001341828.1:p.Thr2486Asn
NM_001354900.1:c.7418C>A	NP_001341829.1:p.Thr2473Asn
NM_001354901.1:c.7364C>A	NP_001341830.1:p.Thr2455Asn
NM_001354902.1:c.7268C>A	NP_001341831.1:p.Thr2423Asn
NM_001354903.1:c.7238C>A	NP_001341832.1:p.Thr2413Asn
NM_001354904.1:c.7163C>A	NP_001341833.1:p.Thr2388Asn
NM_001354905.1:c.7061C>A	NP_001341834.1:p.Thr2354Asn
NM_001354906.1:c.6692C>A	NP_001341835.1:p.Thr2231Asn
NM_000038.6:c.7541C>A MANE Select	NP_000029.2:p.Thr2514Asn
NM_001127510.3:c.7541C>A	NP_001120982.1:p.Thr2514Asn
NM_001127511.3:c.7487C>A	NP_001120983.2:p.Thr2496Asn
NM_001354895.2:c.7541C>A	NP_001341824.1:p.Thr2514Asn
NM_001354896.2:c.7595C>A	NP_001341825.1:p.Thr2532Asn
NM_001354897.2:c.7571C>A	NP_001341826.1:p.Thr2524Asn
NM_001354898.2:c.7466C>A	NP_001341827.1:p.Thr2489Asn
NM_001354899.2:c.7457C>A	NP_001341828.1:p.Thr2486Asn
NM_001354900.2:c.7418C>A	NP_001341829.1:p.Thr2473Asn
NM_001354901.2:c.7364C>A	NP_001341830.1:p.Thr2455Asn
NM_001354902.2:c.7268C>A	NP_001341831.1:p.Thr2423Asn
NM_001354903.2:c.7238C>A	NP_001341832.1:p.Thr2413Asn
NM_001354904.2:c.7163C>A	NP_001341833.1:p.Thr2388Asn
NM_001354905.2:c.7061C>A	NP_001341834.1:p.Thr2354Asn
NM_001354906.2:c.6692C>A	NP_001341835.1:p.Thr2231Asn