Canonical Allele Identifier: CA16025463

Gene: APC

Linked Data

• dbSNP Id: rs587781360
• MyVariant Identifiers: chr5:g.112170799T>G (hg19) ; chr5:g.112835102T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112835102T>G , CM000667.2:g.112835102T>G	GRCh38
NC_000005.9:g.112170799T>G , CM000667.1:g.112170799T>G	GRCh37
NC_000005.8:g.112198698T>G	NCBI36
NG_008481.4:g.147582T>G , LRG_130:g.147582T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1560T>G	ENSP00000484935.2:n.1560T>G
ENST00000504915.3:c.1949T>G	ENSP00000473355.2:p.Ile650Ser
ENST00000505350.2:c.*1901T>G	ENSP00000481752.1:n.*1901T>G
ENST00000507379.6:c.1841T>G	ENSP00000423224.2:p.Ile614Ser
ENST00000509732.6:c.1895T>G	ENSP00000426541.2:p.Ile632Ser
ENST00000512211.7:c.1895T>G	ENSP00000423828.3:p.Ile632Ser
ENST00000257430.9:c.1895T>G MANE Select	ENSP00000257430.4:p.Ile632Ser
ENST00000257430.8:c.1895T>G	ENSP00000257430.4:p.Ile632Ser
ENST00000502371.2:c.248T>G
ENST00000504915.2:c.584T>G	ENSP00000473355.1:p.Ile195Ser
ENST00000507379.5:c.1841T>G	ENSP00000423224.1:p.Ile614Ser
ENST00000508376.6:c.1895T>G	ENSP00000427089.2:p.Ile632Ser
ENST00000508624.5:c.*1217T>G	ENSP00000424265.1:n.*1217T>G
ENST00000512211.6:c.1895T>G	ENSP00000423828.2:p.Ile632Ser
ENST00000520401.1:c.230+6130T>G
NM_000038.5:c.1895T>G	NP_000029.2:p.Ile632Ser
NM_001127510.2:c.1895T>G	NP_001120982.1:p.Ile632Ser
NM_001127511.2:c.1841T>G	NP_001120983.2:p.Ile614Ser
NM_001354895.1:c.1895T>G	NP_001341824.1:p.Ile632Ser
NM_001354896.1:c.1949T>G	NP_001341825.1:p.Ile650Ser
NM_001354897.1:c.1925T>G	NP_001341826.1:p.Ile642Ser
NM_001354898.1:c.1820T>G	NP_001341827.1:p.Ile607Ser
NM_001354899.1:c.1811T>G	NP_001341828.1:p.Ile604Ser
NM_001354900.1:c.1772T>G	NP_001341829.1:p.Ile591Ser
NM_001354901.1:c.1718T>G	NP_001341830.1:p.Ile573Ser
NM_001354902.1:c.1622T>G	NP_001341831.1:p.Ile541Ser
NM_001354903.1:c.1592T>G	NP_001341832.1:p.Ile531Ser
NM_001354904.1:c.1517T>G	NP_001341833.1:p.Ile506Ser
NM_001354905.1:c.1415T>G	NP_001341834.1:p.Ile472Ser
NM_001354906.1:c.1046T>G	NP_001341835.1:p.Ile349Ser
NM_000038.6:c.1895T>G MANE Select	NP_000029.2:p.Ile632Ser
NM_001127510.3:c.1895T>G	NP_001120982.1:p.Ile632Ser
NM_001127511.3:c.1841T>G	NP_001120983.2:p.Ile614Ser
NM_001354895.2:c.1895T>G	NP_001341824.1:p.Ile632Ser
NM_001354896.2:c.1949T>G	NP_001341825.1:p.Ile650Ser
NM_001354897.2:c.1925T>G	NP_001341826.1:p.Ile642Ser
NM_001354898.2:c.1820T>G	NP_001341827.1:p.Ile607Ser
NM_001354899.2:c.1811T>G	NP_001341828.1:p.Ile604Ser
NM_001354900.2:c.1772T>G	NP_001341829.1:p.Ile591Ser
NM_001354901.2:c.1718T>G	NP_001341830.1:p.Ile573Ser
NM_001354902.2:c.1622T>G	NP_001341831.1:p.Ile541Ser
NM_001354903.2:c.1592T>G	NP_001341832.1:p.Ile531Ser
NM_001354904.2:c.1517T>G	NP_001341833.1:p.Ile506Ser
NM_001354905.2:c.1415T>G	NP_001341834.1:p.Ile472Ser
NM_001354906.2:c.1046T>G	NP_001341835.1:p.Ile349Ser