Canonical Allele Identifier: CA16032999

Gene: APC

Linked Data

• dbSNP Id: rs2149937832
• MyVariant Identifiers: chr5:g.112176629C>G (hg19) ; chr5:g.112840932C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840932C>G , CM000667.2:g.112840932C>G	GRCh38
NC_000005.9:g.112176629C>G , CM000667.1:g.112176629C>G	GRCh37
NC_000005.8:g.112204528C>G	NCBI36
NG_008481.4:g.153412C>G , LRG_130:g.153412C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5392C>G	ENSP00000473355.2:p.Pro1798Ala
ENST00000505350.2:c.*5344C>G	ENSP00000481752.1:n.*5344C>G
ENST00000507379.6:c.5284C>G	ENSP00000423224.2:p.Pro1762Ala
ENST00000509732.6:c.5338C>G	ENSP00000426541.2:p.Pro1780Ala
ENST00000512211.7:c.5338C>G	ENSP00000423828.3:p.Pro1780Ala
ENST00000257430.9:c.5338C>G MANE Select	ENSP00000257430.4:p.Pro1780Ala
ENST00000257430.8:c.5338C>G	ENSP00000257430.4:p.Pro1780Ala
ENST00000508376.6:c.5338C>G	ENSP00000427089.2:p.Pro1780Ala
ENST00000508624.5:c.*4660C>G	ENSP00000424265.1:n.*4660C>G
ENST00000520401.1:c.230+11960C>G
NM_000038.5:c.5338C>G	NP_000029.2:p.Pro1780Ala
NM_001127510.2:c.5338C>G	NP_001120982.1:p.Pro1780Ala
NM_001127511.2:c.5284C>G	NP_001120983.2:p.Pro1762Ala
NM_001354895.1:c.5338C>G	NP_001341824.1:p.Pro1780Ala
NM_001354896.1:c.5392C>G	NP_001341825.1:p.Pro1798Ala
NM_001354897.1:c.5368C>G	NP_001341826.1:p.Pro1790Ala
NM_001354898.1:c.5263C>G	NP_001341827.1:p.Pro1755Ala
NM_001354899.1:c.5254C>G	NP_001341828.1:p.Pro1752Ala
NM_001354900.1:c.5215C>G	NP_001341829.1:p.Pro1739Ala
NM_001354901.1:c.5161C>G	NP_001341830.1:p.Pro1721Ala
NM_001354902.1:c.5065C>G	NP_001341831.1:p.Pro1689Ala
NM_001354903.1:c.5035C>G	NP_001341832.1:p.Pro1679Ala
NM_001354904.1:c.4960C>G	NP_001341833.1:p.Pro1654Ala
NM_001354905.1:c.4858C>G	NP_001341834.1:p.Pro1620Ala
NM_001354906.1:c.4489C>G	NP_001341835.1:p.Pro1497Ala
NM_000038.6:c.5338C>G MANE Select	NP_000029.2:p.Pro1780Ala
NM_001127510.3:c.5338C>G	NP_001120982.1:p.Pro1780Ala
NM_001127511.3:c.5284C>G	NP_001120983.2:p.Pro1762Ala
NM_001354895.2:c.5338C>G	NP_001341824.1:p.Pro1780Ala
NM_001354896.2:c.5392C>G	NP_001341825.1:p.Pro1798Ala
NM_001354897.2:c.5368C>G	NP_001341826.1:p.Pro1790Ala
NM_001354898.2:c.5263C>G	NP_001341827.1:p.Pro1755Ala
NM_001354899.2:c.5254C>G	NP_001341828.1:p.Pro1752Ala
NM_001354900.2:c.5215C>G	NP_001341829.1:p.Pro1739Ala
NM_001354901.2:c.5161C>G	NP_001341830.1:p.Pro1721Ala
NM_001354902.2:c.5065C>G	NP_001341831.1:p.Pro1689Ala
NM_001354903.2:c.5035C>G	NP_001341832.1:p.Pro1679Ala
NM_001354904.2:c.4960C>G	NP_001341833.1:p.Pro1654Ala
NM_001354905.2:c.4858C>G	NP_001341834.1:p.Pro1620Ala
NM_001354906.2:c.4489C>G	NP_001341835.1:p.Pro1497Ala