Canonical Allele Identifier: CA005150

Gene: APC

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112827140G>A , CM000667.2:g.112827140G>A	GRCh38
NC_000005.9:g.112162837G>A , CM000667.1:g.112162837G>A	GRCh37
NC_000005.8:g.112190736G>A	NCBI36
NG_008481.4:g.139620G>A , LRG_130:g.139620G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1408+5149G>A	ENSP00000484935.2:n.1408+5149G>A
ENST00000504915.3:c.1495G>A	ENSP00000473355.2:p.Val499Met
ENST00000505084.2:n.1497G>A
ENST00000505350.2:c.*1447G>A	ENSP00000481752.1:n.*1447G>A
ENST00000507379.6:c.1387G>A	ENSP00000423224.2:p.Val463Met
ENST00000509732.6:c.1441G>A	ENSP00000426541.2:p.Val481Met
ENST00000512211.7:c.1441G>A	ENSP00000423828.3:p.Val481Met
ENST00000257430.9:c.1441G>A MANE Select	ENSP00000257430.4:p.Val481Met
ENST00000257430.8:c.1441G>A	ENSP00000257430.4:p.Val481Met
ENST00000502371.2:c.96+5149G>A
ENST00000504915.2:c.130G>A	ENSP00000473355.1:p.Val44Met
ENST00000507379.5:c.1387G>A	ENSP00000423224.1:p.Val463Met
ENST00000508376.6:c.1441G>A	ENSP00000427089.2:p.Val481Met
ENST00000508624.5:c.*763G>A	ENSP00000424265.1:n.*763G>A
ENST00000512211.6:c.1441G>A	ENSP00000423828.2:p.Val481Met
NM_000038.5:c.1441G>A	NP_000029.2:p.Val481Met
NM_001127510.2:c.1441G>A	NP_001120982.1:p.Val481Met
NM_001127511.2:c.1387G>A	NP_001120983.2:p.Val463Met
NM_001354895.1:c.1441G>A	NP_001341824.1:p.Val481Met
NM_001354896.1:c.1495G>A	NP_001341825.1:p.Val499Met
NM_001354897.1:c.1471G>A	NP_001341826.1:p.Val491Met
NM_001354898.1:c.1366G>A	NP_001341827.1:p.Val456Met
NM_001354899.1:c.1357G>A	NP_001341828.1:p.Val453Met
NM_001354900.1:c.1318G>A	NP_001341829.1:p.Val440Met
NM_001354901.1:c.1264G>A	NP_001341830.1:p.Val422Met
NM_001354902.1:c.1168G>A	NP_001341831.1:p.Val390Met
NM_001354903.1:c.1138G>A	NP_001341832.1:p.Val380Met
NM_001354904.1:c.1063G>A	NP_001341833.1:p.Val355Met
NM_001354905.1:c.961G>A	NP_001341834.1:p.Val321Met
NM_001354906.1:c.592G>A	NP_001341835.1:p.Val198Met
NM_000038.6:c.1441G>A MANE Select	NP_000029.2:p.Val481Met
NM_001127510.3:c.1441G>A	NP_001120982.1:p.Val481Met
NM_001127511.3:c.1387G>A	NP_001120983.2:p.Val463Met
NM_001354895.2:c.1441G>A	NP_001341824.1:p.Val481Met
NM_001354896.2:c.1495G>A	NP_001341825.1:p.Val499Met
NM_001354897.2:c.1471G>A	NP_001341826.1:p.Val491Met
NM_001354898.2:c.1366G>A	NP_001341827.1:p.Val456Met
NM_001354899.2:c.1357G>A	NP_001341828.1:p.Val453Met
NM_001354900.2:c.1318G>A	NP_001341829.1:p.Val440Met
NM_001354901.2:c.1264G>A	NP_001341830.1:p.Val422Met
NM_001354902.2:c.1168G>A	NP_001341831.1:p.Val390Met
NM_001354903.2:c.1138G>A	NP_001341832.1:p.Val380Met
NM_001354904.2:c.1063G>A	NP_001341833.1:p.Val355Met
NM_001354905.2:c.961G>A	NP_001341834.1:p.Val321Met
NM_001354906.2:c.592G>A	NP_001341835.1:p.Val198Met