Canonical Allele Identifier: CA16032823

Gene: APC

Linked Data

• dbSNP Id: rs2149935832
• MyVariant Identifiers: chr5:g.112176545C>T (hg19) ; chr5:g.112840848C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840848C>T , CM000667.2:g.112840848C>T	GRCh38
NC_000005.9:g.112176545C>T , CM000667.1:g.112176545C>T	GRCh37
NC_000005.8:g.112204444C>T	NCBI36
NG_008481.4:g.153328C>T , LRG_130:g.153328C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5308C>T	ENSP00000473355.2:p.Gln1770Ter
ENST00000505350.2:c.*5260C>T	ENSP00000481752.1:n.*5260C>T
ENST00000507379.6:c.5200C>T	ENSP00000423224.2:p.Gln1734Ter
ENST00000509732.6:c.5254C>T	ENSP00000426541.2:p.Gln1752Ter
ENST00000512211.7:c.5254C>T	ENSP00000423828.3:p.Gln1752Ter
ENST00000257430.9:c.5254C>T MANE Select	ENSP00000257430.4:p.Gln1752Ter
ENST00000257430.8:c.5254C>T	ENSP00000257430.4:p.Gln1752Ter
ENST00000508376.6:c.5254C>T	ENSP00000427089.2:p.Gln1752Ter
ENST00000508624.5:c.*4576C>T	ENSP00000424265.1:n.*4576C>T
ENST00000520401.1:c.230+11876C>T
NM_000038.5:c.5254C>T	NP_000029.2:p.Gln1752Ter
NM_001127510.2:c.5254C>T	NP_001120982.1:p.Gln1752Ter
NM_001127511.2:c.5200C>T	NP_001120983.2:p.Gln1734Ter
NM_001354895.1:c.5254C>T	NP_001341824.1:p.Gln1752Ter
NM_001354896.1:c.5308C>T	NP_001341825.1:p.Gln1770Ter
NM_001354897.1:c.5284C>T	NP_001341826.1:p.Gln1762Ter
NM_001354898.1:c.5179C>T	NP_001341827.1:p.Gln1727Ter
NM_001354899.1:c.5170C>T	NP_001341828.1:p.Gln1724Ter
NM_001354900.1:c.5131C>T	NP_001341829.1:p.Gln1711Ter
NM_001354901.1:c.5077C>T	NP_001341830.1:p.Gln1693Ter
NM_001354902.1:c.4981C>T	NP_001341831.1:p.Gln1661Ter
NM_001354903.1:c.4951C>T	NP_001341832.1:p.Gln1651Ter
NM_001354904.1:c.4876C>T	NP_001341833.1:p.Gln1626Ter
NM_001354905.1:c.4774C>T	NP_001341834.1:p.Gln1592Ter
NM_001354906.1:c.4405C>T	NP_001341835.1:p.Gln1469Ter
NM_000038.6:c.5254C>T MANE Select	NP_000029.2:p.Gln1752Ter
NM_001127510.3:c.5254C>T	NP_001120982.1:p.Gln1752Ter
NM_001127511.3:c.5200C>T	NP_001120983.2:p.Gln1734Ter
NM_001354895.2:c.5254C>T	NP_001341824.1:p.Gln1752Ter
NM_001354896.2:c.5308C>T	NP_001341825.1:p.Gln1770Ter
NM_001354897.2:c.5284C>T	NP_001341826.1:p.Gln1762Ter
NM_001354898.2:c.5179C>T	NP_001341827.1:p.Gln1727Ter
NM_001354899.2:c.5170C>T	NP_001341828.1:p.Gln1724Ter
NM_001354900.2:c.5131C>T	NP_001341829.1:p.Gln1711Ter
NM_001354901.2:c.5077C>T	NP_001341830.1:p.Gln1693Ter
NM_001354902.2:c.4981C>T	NP_001341831.1:p.Gln1661Ter
NM_001354903.2:c.4951C>T	NP_001341832.1:p.Gln1651Ter
NM_001354904.2:c.4876C>T	NP_001341833.1:p.Gln1626Ter
NM_001354905.2:c.4774C>T	NP_001341834.1:p.Gln1592Ter
NM_001354906.2:c.4405C>T	NP_001341835.1:p.Gln1469Ter