Canonical Allele Identifier: CA16033739

Gene: APC

Linked Data

• ClinVar Variation Id: 653946
• ClinVar RCV Id: RCV003768513
• dbSNP Id: rs1580662288
• MyVariant Identifiers: chr5:g.112176957A>G (hg19) ; chr5:g.112841260A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112841260A>G , CM000667.2:g.112841260A>G	GRCh38
NC_000005.9:g.112176957A>G , CM000667.1:g.112176957A>G	GRCh37
NC_000005.8:g.112204856A>G	NCBI36
NG_008481.4:g.153740A>G , LRG_130:g.153740A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5720A>G	ENSP00000473355.2:p.Glu1907Gly
ENST00000505350.2:c.*5672A>G	ENSP00000481752.1:n.*5672A>G
ENST00000507379.6:c.5612A>G	ENSP00000423224.2:p.Glu1871Gly
ENST00000509732.6:c.5666A>G	ENSP00000426541.2:p.Glu1889Gly
ENST00000512211.7:c.5666A>G	ENSP00000423828.3:p.Glu1889Gly
ENST00000257430.9:c.5666A>G MANE Select	ENSP00000257430.4:p.Glu1889Gly
ENST00000257430.8:c.5666A>G	ENSP00000257430.4:p.Glu1889Gly
ENST00000508376.6:c.5666A>G	ENSP00000427089.2:p.Glu1889Gly
ENST00000508624.5:c.*4988A>G	ENSP00000424265.1:n.*4988A>G
ENST00000520401.1:c.230+12288A>G
NM_000038.5:c.5666A>G	NP_000029.2:p.Glu1889Gly
NM_001127510.2:c.5666A>G	NP_001120982.1:p.Glu1889Gly
NM_001127511.2:c.5612A>G	NP_001120983.2:p.Glu1871Gly
NM_001354895.1:c.5666A>G	NP_001341824.1:p.Glu1889Gly
NM_001354896.1:c.5720A>G	NP_001341825.1:p.Glu1907Gly
NM_001354897.1:c.5696A>G	NP_001341826.1:p.Glu1899Gly
NM_001354898.1:c.5591A>G	NP_001341827.1:p.Glu1864Gly
NM_001354899.1:c.5582A>G	NP_001341828.1:p.Glu1861Gly
NM_001354900.1:c.5543A>G	NP_001341829.1:p.Glu1848Gly
NM_001354901.1:c.5489A>G	NP_001341830.1:p.Glu1830Gly
NM_001354902.1:c.5393A>G	NP_001341831.1:p.Glu1798Gly
NM_001354903.1:c.5363A>G	NP_001341832.1:p.Glu1788Gly
NM_001354904.1:c.5288A>G	NP_001341833.1:p.Glu1763Gly
NM_001354905.1:c.5186A>G	NP_001341834.1:p.Glu1729Gly
NM_001354906.1:c.4817A>G	NP_001341835.1:p.Glu1606Gly
NM_000038.6:c.5666A>G MANE Select	NP_000029.2:p.Glu1889Gly
NM_001127510.3:c.5666A>G	NP_001120982.1:p.Glu1889Gly
NM_001127511.3:c.5612A>G	NP_001120983.2:p.Glu1871Gly
NM_001354895.2:c.5666A>G	NP_001341824.1:p.Glu1889Gly
NM_001354896.2:c.5720A>G	NP_001341825.1:p.Glu1907Gly
NM_001354897.2:c.5696A>G	NP_001341826.1:p.Glu1899Gly
NM_001354898.2:c.5591A>G	NP_001341827.1:p.Glu1864Gly
NM_001354899.2:c.5582A>G	NP_001341828.1:p.Glu1861Gly
NM_001354900.2:c.5543A>G	NP_001341829.1:p.Glu1848Gly
NM_001354901.2:c.5489A>G	NP_001341830.1:p.Glu1830Gly
NM_001354902.2:c.5393A>G	NP_001341831.1:p.Glu1798Gly
NM_001354903.2:c.5363A>G	NP_001341832.1:p.Glu1788Gly
NM_001354904.2:c.5288A>G	NP_001341833.1:p.Glu1763Gly
NM_001354905.2:c.5186A>G	NP_001341834.1:p.Glu1729Gly
NM_001354906.2:c.4817A>G	NP_001341835.1:p.Glu1606Gly