Canonical Allele Identifier: CA16038029

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112178979C>G (hg19) ; chr5:g.112843282C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843282C>G , CM000667.2:g.112843282C>G	GRCh38
NC_000005.9:g.112178979C>G , CM000667.1:g.112178979C>G	GRCh37
NC_000005.8:g.112206878C>G	NCBI36
NG_008481.4:g.155762C>G , LRG_130:g.155762C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7742C>G	ENSP00000473355.2:p.Thr2581Ser
ENST00000505350.2:c.*7694C>G	ENSP00000481752.1:n.*7694C>G
ENST00000507379.6:c.7634C>G	ENSP00000423224.2:p.Thr2545Ser
ENST00000509732.6:c.7688C>G	ENSP00000426541.2:p.Thr2563Ser
ENST00000512211.7:c.7688C>G	ENSP00000423828.3:p.Thr2563Ser
ENST00000257430.9:c.7688C>G MANE Select	ENSP00000257430.4:p.Thr2563Ser
ENST00000257430.8:c.7688C>G	ENSP00000257430.4:p.Thr2563Ser
ENST00000508376.6:c.7688C>G	ENSP00000427089.2:p.Thr2563Ser
ENST00000520401.1:c.231-13367C>G
NM_000038.5:c.7688C>G	NP_000029.2:p.Thr2563Ser
NM_001127510.2:c.7688C>G	NP_001120982.1:p.Thr2563Ser
NM_001127511.2:c.7634C>G	NP_001120983.2:p.Thr2545Ser
NM_001354895.1:c.7688C>G	NP_001341824.1:p.Thr2563Ser
NM_001354896.1:c.7742C>G	NP_001341825.1:p.Thr2581Ser
NM_001354897.1:c.7718C>G	NP_001341826.1:p.Thr2573Ser
NM_001354898.1:c.7613C>G	NP_001341827.1:p.Thr2538Ser
NM_001354899.1:c.7604C>G	NP_001341828.1:p.Thr2535Ser
NM_001354900.1:c.7565C>G	NP_001341829.1:p.Thr2522Ser
NM_001354901.1:c.7511C>G	NP_001341830.1:p.Thr2504Ser
NM_001354902.1:c.7415C>G	NP_001341831.1:p.Thr2472Ser
NM_001354903.1:c.7385C>G	NP_001341832.1:p.Thr2462Ser
NM_001354904.1:c.7310C>G	NP_001341833.1:p.Thr2437Ser
NM_001354905.1:c.7208C>G	NP_001341834.1:p.Thr2403Ser
NM_001354906.1:c.6839C>G	NP_001341835.1:p.Thr2280Ser
NM_000038.6:c.7688C>G MANE Select	NP_000029.2:p.Thr2563Ser
NM_001127510.3:c.7688C>G	NP_001120982.1:p.Thr2563Ser
NM_001127511.3:c.7634C>G	NP_001120983.2:p.Thr2545Ser
NM_001354895.2:c.7688C>G	NP_001341824.1:p.Thr2563Ser
NM_001354896.2:c.7742C>G	NP_001341825.1:p.Thr2581Ser
NM_001354897.2:c.7718C>G	NP_001341826.1:p.Thr2573Ser
NM_001354898.2:c.7613C>G	NP_001341827.1:p.Thr2538Ser
NM_001354899.2:c.7604C>G	NP_001341828.1:p.Thr2535Ser
NM_001354900.2:c.7565C>G	NP_001341829.1:p.Thr2522Ser
NM_001354901.2:c.7511C>G	NP_001341830.1:p.Thr2504Ser
NM_001354902.2:c.7415C>G	NP_001341831.1:p.Thr2472Ser
NM_001354903.2:c.7385C>G	NP_001341832.1:p.Thr2462Ser
NM_001354904.2:c.7310C>G	NP_001341833.1:p.Thr2437Ser
NM_001354905.2:c.7208C>G	NP_001341834.1:p.Thr2403Ser
NM_001354906.2:c.6839C>G	NP_001341835.1:p.Thr2280Ser