Canonical Allele Identifier: CA16033854

Gene: APC

Linked Data

• ClinVar Variation Id: 1749285
• ClinVar RCV Id: RCV002347685
• dbSNP Id: rs573184569
• MyVariant Identifiers: chr5:g.112177011C>G (hg19) ; chr5:g.112841314C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112841314C>G , CM000667.2:g.112841314C>G	GRCh38
NC_000005.9:g.112177011C>G , CM000667.1:g.112177011C>G	GRCh37
NC_000005.8:g.112204910C>G	NCBI36
NG_008481.4:g.153794C>G , LRG_130:g.153794C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5774C>G	ENSP00000473355.2:p.Ala1925Gly
ENST00000505350.2:c.*5726C>G	ENSP00000481752.1:n.*5726C>G
ENST00000507379.6:c.5666C>G	ENSP00000423224.2:p.Ala1889Gly
ENST00000509732.6:c.5720C>G	ENSP00000426541.2:p.Ala1907Gly
ENST00000512211.7:c.5720C>G	ENSP00000423828.3:p.Ala1907Gly
ENST00000257430.9:c.5720C>G MANE Select	ENSP00000257430.4:p.Ala1907Gly
ENST00000257430.8:c.5720C>G	ENSP00000257430.4:p.Ala1907Gly
ENST00000508376.6:c.5720C>G	ENSP00000427089.2:p.Ala1907Gly
ENST00000508624.5:c.*5042C>G	ENSP00000424265.1:n.*5042C>G
ENST00000520401.1:c.230+12342C>G
NM_000038.5:c.5720C>G	NP_000029.2:p.Ala1907Gly
NM_001127510.2:c.5720C>G	NP_001120982.1:p.Ala1907Gly
NM_001127511.2:c.5666C>G	NP_001120983.2:p.Ala1889Gly
NM_001354895.1:c.5720C>G	NP_001341824.1:p.Ala1907Gly
NM_001354896.1:c.5774C>G	NP_001341825.1:p.Ala1925Gly
NM_001354897.1:c.5750C>G	NP_001341826.1:p.Ala1917Gly
NM_001354898.1:c.5645C>G	NP_001341827.1:p.Ala1882Gly
NM_001354899.1:c.5636C>G	NP_001341828.1:p.Ala1879Gly
NM_001354900.1:c.5597C>G	NP_001341829.1:p.Ala1866Gly
NM_001354901.1:c.5543C>G	NP_001341830.1:p.Ala1848Gly
NM_001354902.1:c.5447C>G	NP_001341831.1:p.Ala1816Gly
NM_001354903.1:c.5417C>G	NP_001341832.1:p.Ala1806Gly
NM_001354904.1:c.5342C>G	NP_001341833.1:p.Ala1781Gly
NM_001354905.1:c.5240C>G	NP_001341834.1:p.Ala1747Gly
NM_001354906.1:c.4871C>G	NP_001341835.1:p.Ala1624Gly
NM_000038.6:c.5720C>G MANE Select	NP_000029.2:p.Ala1907Gly
NM_001127510.3:c.5720C>G	NP_001120982.1:p.Ala1907Gly
NM_001127511.3:c.5666C>G	NP_001120983.2:p.Ala1889Gly
NM_001354895.2:c.5720C>G	NP_001341824.1:p.Ala1907Gly
NM_001354896.2:c.5774C>G	NP_001341825.1:p.Ala1925Gly
NM_001354897.2:c.5750C>G	NP_001341826.1:p.Ala1917Gly
NM_001354898.2:c.5645C>G	NP_001341827.1:p.Ala1882Gly
NM_001354899.2:c.5636C>G	NP_001341828.1:p.Ala1879Gly
NM_001354900.2:c.5597C>G	NP_001341829.1:p.Ala1866Gly
NM_001354901.2:c.5543C>G	NP_001341830.1:p.Ala1848Gly
NM_001354902.2:c.5447C>G	NP_001341831.1:p.Ala1816Gly
NM_001354903.2:c.5417C>G	NP_001341832.1:p.Ala1806Gly
NM_001354904.2:c.5342C>G	NP_001341833.1:p.Ala1781Gly
NM_001354905.2:c.5240C>G	NP_001341834.1:p.Ala1747Gly
NM_001354906.2:c.4871C>G	NP_001341835.1:p.Ala1624Gly