Canonical Allele Identifier: CA16031772

Gene: APC

Linked Data

• dbSNP Id: rs879131155
• MyVariant Identifiers: chr5:g.112176053T>A (hg19) ; chr5:g.112840356T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840356T>A , CM000667.2:g.112840356T>A	GRCh38
NC_000005.9:g.112176053T>A , CM000667.1:g.112176053T>A	GRCh37
NC_000005.8:g.112203952T>A	NCBI36
NG_008481.4:g.152836T>A , LRG_130:g.152836T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4816T>A	ENSP00000473355.2:p.Ser1606Thr
ENST00000505350.2:c.*4768T>A	ENSP00000481752.1:n.*4768T>A
ENST00000507379.6:c.4708T>A	ENSP00000423224.2:p.Ser1570Thr
ENST00000509732.6:c.4762T>A	ENSP00000426541.2:p.Ser1588Thr
ENST00000512211.7:c.4762T>A	ENSP00000423828.3:p.Ser1588Thr
ENST00000257430.9:c.4762T>A MANE Select	ENSP00000257430.4:p.Ser1588Thr
ENST00000257430.8:c.4762T>A	ENSP00000257430.4:p.Ser1588Thr
ENST00000508376.6:c.4762T>A	ENSP00000427089.2:p.Ser1588Thr
ENST00000508624.5:c.*4084T>A	ENSP00000424265.1:n.*4084T>A
ENST00000520401.1:c.230+11384T>A
NM_000038.5:c.4762T>A	NP_000029.2:p.Ser1588Thr
NM_001127510.2:c.4762T>A	NP_001120982.1:p.Ser1588Thr
NM_001127511.2:c.4708T>A	NP_001120983.2:p.Ser1570Thr
NM_001354895.1:c.4762T>A	NP_001341824.1:p.Ser1588Thr
NM_001354896.1:c.4816T>A	NP_001341825.1:p.Ser1606Thr
NM_001354897.1:c.4792T>A	NP_001341826.1:p.Ser1598Thr
NM_001354898.1:c.4687T>A	NP_001341827.1:p.Ser1563Thr
NM_001354899.1:c.4678T>A	NP_001341828.1:p.Ser1560Thr
NM_001354900.1:c.4639T>A	NP_001341829.1:p.Ser1547Thr
NM_001354901.1:c.4585T>A	NP_001341830.1:p.Ser1529Thr
NM_001354902.1:c.4489T>A	NP_001341831.1:p.Ser1497Thr
NM_001354903.1:c.4459T>A	NP_001341832.1:p.Ser1487Thr
NM_001354904.1:c.4384T>A	NP_001341833.1:p.Ser1462Thr
NM_001354905.1:c.4282T>A	NP_001341834.1:p.Ser1428Thr
NM_001354906.1:c.3913T>A	NP_001341835.1:p.Ser1305Thr
NM_000038.6:c.4762T>A MANE Select	NP_000029.2:p.Ser1588Thr
NM_001127510.3:c.4762T>A	NP_001120982.1:p.Ser1588Thr
NM_001127511.3:c.4708T>A	NP_001120983.2:p.Ser1570Thr
NM_001354895.2:c.4762T>A	NP_001341824.1:p.Ser1588Thr
NM_001354896.2:c.4816T>A	NP_001341825.1:p.Ser1606Thr
NM_001354897.2:c.4792T>A	NP_001341826.1:p.Ser1598Thr
NM_001354898.2:c.4687T>A	NP_001341827.1:p.Ser1563Thr
NM_001354899.2:c.4678T>A	NP_001341828.1:p.Ser1560Thr
NM_001354900.2:c.4639T>A	NP_001341829.1:p.Ser1547Thr
NM_001354901.2:c.4585T>A	NP_001341830.1:p.Ser1529Thr
NM_001354902.2:c.4489T>A	NP_001341831.1:p.Ser1497Thr
NM_001354903.2:c.4459T>A	NP_001341832.1:p.Ser1487Thr
NM_001354904.2:c.4384T>A	NP_001341833.1:p.Ser1462Thr
NM_001354905.2:c.4282T>A	NP_001341834.1:p.Ser1428Thr
NM_001354906.2:c.3913T>A	NP_001341835.1:p.Ser1305Thr