Canonical Allele Identifier: CA16032843

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112176557T>A (hg19) ; chr5:g.112840860T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840860T>A , CM000667.2:g.112840860T>A	GRCh38
NC_000005.9:g.112176557T>A , CM000667.1:g.112176557T>A	GRCh37
NC_000005.8:g.112204456T>A	NCBI36
NG_008481.4:g.153340T>A , LRG_130:g.153340T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5320T>A	ENSP00000473355.2:p.Ser1774Thr
ENST00000505350.2:c.*5272T>A	ENSP00000481752.1:n.*5272T>A
ENST00000507379.6:c.5212T>A	ENSP00000423224.2:p.Ser1738Thr
ENST00000509732.6:c.5266T>A	ENSP00000426541.2:p.Ser1756Thr
ENST00000512211.7:c.5266T>A	ENSP00000423828.3:p.Ser1756Thr
ENST00000257430.9:c.5266T>A MANE Select	ENSP00000257430.4:p.Ser1756Thr
ENST00000257430.8:c.5266T>A	ENSP00000257430.4:p.Ser1756Thr
ENST00000508376.6:c.5266T>A	ENSP00000427089.2:p.Ser1756Thr
ENST00000508624.5:c.*4588T>A	ENSP00000424265.1:n.*4588T>A
ENST00000520401.1:c.230+11888T>A
NM_000038.5:c.5266T>A	NP_000029.2:p.Ser1756Thr
NM_001127510.2:c.5266T>A	NP_001120982.1:p.Ser1756Thr
NM_001127511.2:c.5212T>A	NP_001120983.2:p.Ser1738Thr
NM_001354895.1:c.5266T>A	NP_001341824.1:p.Ser1756Thr
NM_001354896.1:c.5320T>A	NP_001341825.1:p.Ser1774Thr
NM_001354897.1:c.5296T>A	NP_001341826.1:p.Ser1766Thr
NM_001354898.1:c.5191T>A	NP_001341827.1:p.Ser1731Thr
NM_001354899.1:c.5182T>A	NP_001341828.1:p.Ser1728Thr
NM_001354900.1:c.5143T>A	NP_001341829.1:p.Ser1715Thr
NM_001354901.1:c.5089T>A	NP_001341830.1:p.Ser1697Thr
NM_001354902.1:c.4993T>A	NP_001341831.1:p.Ser1665Thr
NM_001354903.1:c.4963T>A	NP_001341832.1:p.Ser1655Thr
NM_001354904.1:c.4888T>A	NP_001341833.1:p.Ser1630Thr
NM_001354905.1:c.4786T>A	NP_001341834.1:p.Ser1596Thr
NM_001354906.1:c.4417T>A	NP_001341835.1:p.Ser1473Thr
NM_000038.6:c.5266T>A MANE Select	NP_000029.2:p.Ser1756Thr
NM_001127510.3:c.5266T>A	NP_001120982.1:p.Ser1756Thr
NM_001127511.3:c.5212T>A	NP_001120983.2:p.Ser1738Thr
NM_001354895.2:c.5266T>A	NP_001341824.1:p.Ser1756Thr
NM_001354896.2:c.5320T>A	NP_001341825.1:p.Ser1774Thr
NM_001354897.2:c.5296T>A	NP_001341826.1:p.Ser1766Thr
NM_001354898.2:c.5191T>A	NP_001341827.1:p.Ser1731Thr
NM_001354899.2:c.5182T>A	NP_001341828.1:p.Ser1728Thr
NM_001354900.2:c.5143T>A	NP_001341829.1:p.Ser1715Thr
NM_001354901.2:c.5089T>A	NP_001341830.1:p.Ser1697Thr
NM_001354902.2:c.4993T>A	NP_001341831.1:p.Ser1665Thr
NM_001354903.2:c.4963T>A	NP_001341832.1:p.Ser1655Thr
NM_001354904.2:c.4888T>A	NP_001341833.1:p.Ser1630Thr
NM_001354905.2:c.4786T>A	NP_001341834.1:p.Ser1596Thr
NM_001354906.2:c.4417T>A	NP_001341835.1:p.Ser1473Thr