Canonical Allele Identifier: CA16024511

Gene: APC

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112827164A>C , CM000667.2:g.112827164A>C	GRCh38
NC_000005.9:g.112162861A>C , CM000667.1:g.112162861A>C	GRCh37
NC_000005.8:g.112190760A>C	NCBI36
NG_008481.4:g.139644A>C , LRG_130:g.139644A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1408+5173A>C	ENSP00000484935.2:n.1408+5173A>C
ENST00000504915.3:c.1519A>C	ENSP00000473355.2:p.Thr507Pro
ENST00000505084.2:n.1521A>C
ENST00000505350.2:c.*1471A>C	ENSP00000481752.1:n.*1471A>C
ENST00000507379.6:c.1411A>C	ENSP00000423224.2:p.Thr471Pro
ENST00000509732.6:c.1465A>C	ENSP00000426541.2:p.Thr489Pro
ENST00000512211.7:c.1465A>C	ENSP00000423828.3:p.Thr489Pro
ENST00000257430.9:c.1465A>C MANE Select	ENSP00000257430.4:p.Thr489Pro
ENST00000257430.8:c.1465A>C	ENSP00000257430.4:p.Thr489Pro
ENST00000502371.2:c.96+5173A>C
ENST00000504915.2:c.154A>C	ENSP00000473355.1:p.Thr52Pro
ENST00000507379.5:c.1411A>C	ENSP00000423224.1:p.Thr471Pro
ENST00000508376.6:c.1465A>C	ENSP00000427089.2:p.Thr489Pro
ENST00000508624.5:c.*787A>C	ENSP00000424265.1:n.*787A>C
ENST00000512211.6:c.1465A>C	ENSP00000423828.2:p.Thr489Pro
NM_000038.5:c.1465A>C	NP_000029.2:p.Thr489Pro
NM_001127510.2:c.1465A>C	NP_001120982.1:p.Thr489Pro
NM_001127511.2:c.1411A>C	NP_001120983.2:p.Thr471Pro
NM_001354895.1:c.1465A>C	NP_001341824.1:p.Thr489Pro
NM_001354896.1:c.1519A>C	NP_001341825.1:p.Thr507Pro
NM_001354897.1:c.1495A>C	NP_001341826.1:p.Thr499Pro
NM_001354898.1:c.1390A>C	NP_001341827.1:p.Thr464Pro
NM_001354899.1:c.1381A>C	NP_001341828.1:p.Thr461Pro
NM_001354900.1:c.1342A>C	NP_001341829.1:p.Thr448Pro
NM_001354901.1:c.1288A>C	NP_001341830.1:p.Thr430Pro
NM_001354902.1:c.1192A>C	NP_001341831.1:p.Thr398Pro
NM_001354903.1:c.1162A>C	NP_001341832.1:p.Thr388Pro
NM_001354904.1:c.1087A>C	NP_001341833.1:p.Thr363Pro
NM_001354905.1:c.985A>C	NP_001341834.1:p.Thr329Pro
NM_001354906.1:c.616A>C	NP_001341835.1:p.Thr206Pro
NM_000038.6:c.1465A>C MANE Select	NP_000029.2:p.Thr489Pro
NM_001127510.3:c.1465A>C	NP_001120982.1:p.Thr489Pro
NM_001127511.3:c.1411A>C	NP_001120983.2:p.Thr471Pro
NM_001354895.2:c.1465A>C	NP_001341824.1:p.Thr489Pro
NM_001354896.2:c.1519A>C	NP_001341825.1:p.Thr507Pro
NM_001354897.2:c.1495A>C	NP_001341826.1:p.Thr499Pro
NM_001354898.2:c.1390A>C	NP_001341827.1:p.Thr464Pro
NM_001354899.2:c.1381A>C	NP_001341828.1:p.Thr461Pro
NM_001354900.2:c.1342A>C	NP_001341829.1:p.Thr448Pro
NM_001354901.2:c.1288A>C	NP_001341830.1:p.Thr430Pro
NM_001354902.2:c.1192A>C	NP_001341831.1:p.Thr398Pro
NM_001354903.2:c.1162A>C	NP_001341832.1:p.Thr388Pro
NM_001354904.2:c.1087A>C	NP_001341833.1:p.Thr363Pro
NM_001354905.2:c.985A>C	NP_001341834.1:p.Thr329Pro
NM_001354906.2:c.616A>C	NP_001341835.1:p.Thr206Pro