Canonical Allele Identifier: CA16031732

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112176033C>A (hg19) ; chr5:g.112840336C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840336C>A , CM000667.2:g.112840336C>A	GRCh38
NC_000005.9:g.112176033C>A , CM000667.1:g.112176033C>A	GRCh37
NC_000005.8:g.112203932C>A	NCBI36
NG_008481.4:g.152816C>A , LRG_130:g.152816C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4796C>A	ENSP00000473355.2:p.Ser1599Tyr
ENST00000505350.2:c.*4748C>A	ENSP00000481752.1:n.*4748C>A
ENST00000507379.6:c.4688C>A	ENSP00000423224.2:p.Ser1563Tyr
ENST00000509732.6:c.4742C>A	ENSP00000426541.2:p.Ser1581Tyr
ENST00000512211.7:c.4742C>A	ENSP00000423828.3:p.Ser1581Tyr
ENST00000257430.9:c.4742C>A MANE Select	ENSP00000257430.4:p.Ser1581Tyr
ENST00000257430.8:c.4742C>A	ENSP00000257430.4:p.Ser1581Tyr
ENST00000508376.6:c.4742C>A	ENSP00000427089.2:p.Ser1581Tyr
ENST00000508624.5:c.*4064C>A	ENSP00000424265.1:n.*4064C>A
ENST00000520401.1:c.230+11364C>A
NM_000038.5:c.4742C>A	NP_000029.2:p.Ser1581Tyr
NM_001127510.2:c.4742C>A	NP_001120982.1:p.Ser1581Tyr
NM_001127511.2:c.4688C>A	NP_001120983.2:p.Ser1563Tyr
NM_001354895.1:c.4742C>A	NP_001341824.1:p.Ser1581Tyr
NM_001354896.1:c.4796C>A	NP_001341825.1:p.Ser1599Tyr
NM_001354897.1:c.4772C>A	NP_001341826.1:p.Ser1591Tyr
NM_001354898.1:c.4667C>A	NP_001341827.1:p.Ser1556Tyr
NM_001354899.1:c.4658C>A	NP_001341828.1:p.Ser1553Tyr
NM_001354900.1:c.4619C>A	NP_001341829.1:p.Ser1540Tyr
NM_001354901.1:c.4565C>A	NP_001341830.1:p.Ser1522Tyr
NM_001354902.1:c.4469C>A	NP_001341831.1:p.Ser1490Tyr
NM_001354903.1:c.4439C>A	NP_001341832.1:p.Ser1480Tyr
NM_001354904.1:c.4364C>A	NP_001341833.1:p.Ser1455Tyr
NM_001354905.1:c.4262C>A	NP_001341834.1:p.Ser1421Tyr
NM_001354906.1:c.3893C>A	NP_001341835.1:p.Ser1298Tyr
NM_000038.6:c.4742C>A MANE Select	NP_000029.2:p.Ser1581Tyr
NM_001127510.3:c.4742C>A	NP_001120982.1:p.Ser1581Tyr
NM_001127511.3:c.4688C>A	NP_001120983.2:p.Ser1563Tyr
NM_001354895.2:c.4742C>A	NP_001341824.1:p.Ser1581Tyr
NM_001354896.2:c.4796C>A	NP_001341825.1:p.Ser1599Tyr
NM_001354897.2:c.4772C>A	NP_001341826.1:p.Ser1591Tyr
NM_001354898.2:c.4667C>A	NP_001341827.1:p.Ser1556Tyr
NM_001354899.2:c.4658C>A	NP_001341828.1:p.Ser1553Tyr
NM_001354900.2:c.4619C>A	NP_001341829.1:p.Ser1540Tyr
NM_001354901.2:c.4565C>A	NP_001341830.1:p.Ser1522Tyr
NM_001354902.2:c.4469C>A	NP_001341831.1:p.Ser1490Tyr
NM_001354903.2:c.4439C>A	NP_001341832.1:p.Ser1480Tyr
NM_001354904.2:c.4364C>A	NP_001341833.1:p.Ser1455Tyr
NM_001354905.2:c.4262C>A	NP_001341834.1:p.Ser1421Tyr
NM_001354906.2:c.3893C>A	NP_001341835.1:p.Ser1298Tyr