Canonical Allele Identifier: CA027893

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112827182A>G , CM000667.2:g.112827182A>G	GRCh38
NC_000005.9:g.112162879A>G , CM000667.1:g.112162879A>G	GRCh37
NC_000005.8:g.112190778A>G	NCBI36
NG_008481.4:g.139662A>G , LRG_130:g.139662A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1408+5191A>G	ENSP00000484935.2:n.1408+5191A>G
ENST00000504915.3:c.1537A>G	ENSP00000473355.2:p.Ile513Val
ENST00000505084.2:n.1539A>G
ENST00000505350.2:c.*1489A>G	ENSP00000481752.1:n.*1489A>G
ENST00000507379.6:c.1429A>G	ENSP00000423224.2:p.Ile477Val
ENST00000509732.6:c.1483A>G	ENSP00000426541.2:p.Ile495Val
ENST00000512211.7:c.1483A>G	ENSP00000423828.3:p.Ile495Val
ENST00000257430.9:c.1483A>G MANE Select	ENSP00000257430.4:p.Ile495Val
ENST00000257430.8:c.1483A>G	ENSP00000257430.4:p.Ile495Val
ENST00000502371.2:c.96+5191A>G
ENST00000504915.2:c.172A>G	ENSP00000473355.1:p.Ile58Val
ENST00000507379.5:c.1429A>G	ENSP00000423224.1:p.Ile477Val
ENST00000508376.6:c.1483A>G	ENSP00000427089.2:p.Ile495Val
ENST00000508624.5:c.*805A>G	ENSP00000424265.1:n.*805A>G
ENST00000512211.6:c.1483A>G	ENSP00000423828.2:p.Ile495Val
NM_000038.5:c.1483A>G	NP_000029.2:p.Ile495Val
NM_001127510.2:c.1483A>G	NP_001120982.1:p.Ile495Val
NM_001127511.2:c.1429A>G	NP_001120983.2:p.Ile477Val
NM_001354895.1:c.1483A>G	NP_001341824.1:p.Ile495Val
NM_001354896.1:c.1537A>G	NP_001341825.1:p.Ile513Val
NM_001354897.1:c.1513A>G	NP_001341826.1:p.Ile505Val
NM_001354898.1:c.1408A>G	NP_001341827.1:p.Ile470Val
NM_001354899.1:c.1399A>G	NP_001341828.1:p.Ile467Val
NM_001354900.1:c.1360A>G	NP_001341829.1:p.Ile454Val
NM_001354901.1:c.1306A>G	NP_001341830.1:p.Ile436Val
NM_001354902.1:c.1210A>G	NP_001341831.1:p.Ile404Val
NM_001354903.1:c.1180A>G	NP_001341832.1:p.Ile394Val
NM_001354904.1:c.1105A>G	NP_001341833.1:p.Ile369Val
NM_001354905.1:c.1003A>G	NP_001341834.1:p.Ile335Val
NM_001354906.1:c.634A>G	NP_001341835.1:p.Ile212Val
NM_000038.6:c.1483A>G MANE Select	NP_000029.2:p.Ile495Val
NM_001127510.3:c.1483A>G	NP_001120982.1:p.Ile495Val
NM_001127511.3:c.1429A>G	NP_001120983.2:p.Ile477Val
NM_001354895.2:c.1483A>G	NP_001341824.1:p.Ile495Val
NM_001354896.2:c.1537A>G	NP_001341825.1:p.Ile513Val
NM_001354897.2:c.1513A>G	NP_001341826.1:p.Ile505Val
NM_001354898.2:c.1408A>G	NP_001341827.1:p.Ile470Val
NM_001354899.2:c.1399A>G	NP_001341828.1:p.Ile467Val
NM_001354900.2:c.1360A>G	NP_001341829.1:p.Ile454Val
NM_001354901.2:c.1306A>G	NP_001341830.1:p.Ile436Val
NM_001354902.2:c.1210A>G	NP_001341831.1:p.Ile404Val
NM_001354903.2:c.1180A>G	NP_001341832.1:p.Ile394Val
NM_001354904.2:c.1105A>G	NP_001341833.1:p.Ile369Val
NM_001354905.2:c.1003A>G	NP_001341834.1:p.Ile335Val
NM_001354906.2:c.634A>G	NP_001341835.1:p.Ile212Val