Canonical Allele Identifier: CA16032411

Gene: APC

Linked Data

• dbSNP Id: rs551084068
• MyVariant Identifiers: chr5:g.112176357C>G (hg19) ; chr5:g.112840660C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840660C>G , CM000667.2:g.112840660C>G	GRCh38
NC_000005.9:g.112176357C>G , CM000667.1:g.112176357C>G	GRCh37
NC_000005.8:g.112204256C>G	NCBI36
NG_008481.4:g.153140C>G , LRG_130:g.153140C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5120C>G	ENSP00000473355.2:p.Thr1707Ser
ENST00000505350.2:c.*5072C>G	ENSP00000481752.1:n.*5072C>G
ENST00000507379.6:c.5012C>G	ENSP00000423224.2:p.Thr1671Ser
ENST00000509732.6:c.5066C>G	ENSP00000426541.2:p.Thr1689Ser
ENST00000512211.7:c.5066C>G	ENSP00000423828.3:p.Thr1689Ser
ENST00000257430.9:c.5066C>G MANE Select	ENSP00000257430.4:p.Thr1689Ser
ENST00000257430.8:c.5066C>G	ENSP00000257430.4:p.Thr1689Ser
ENST00000508376.6:c.5066C>G	ENSP00000427089.2:p.Thr1689Ser
ENST00000508624.5:c.*4388C>G	ENSP00000424265.1:n.*4388C>G
ENST00000520401.1:c.230+11688C>G
NM_000038.5:c.5066C>G	NP_000029.2:p.Thr1689Ser
NM_001127510.2:c.5066C>G	NP_001120982.1:p.Thr1689Ser
NM_001127511.2:c.5012C>G	NP_001120983.2:p.Thr1671Ser
NM_001354895.1:c.5066C>G	NP_001341824.1:p.Thr1689Ser
NM_001354896.1:c.5120C>G	NP_001341825.1:p.Thr1707Ser
NM_001354897.1:c.5096C>G	NP_001341826.1:p.Thr1699Ser
NM_001354898.1:c.4991C>G	NP_001341827.1:p.Thr1664Ser
NM_001354899.1:c.4982C>G	NP_001341828.1:p.Thr1661Ser
NM_001354900.1:c.4943C>G	NP_001341829.1:p.Thr1648Ser
NM_001354901.1:c.4889C>G	NP_001341830.1:p.Thr1630Ser
NM_001354902.1:c.4793C>G	NP_001341831.1:p.Thr1598Ser
NM_001354903.1:c.4763C>G	NP_001341832.1:p.Thr1588Ser
NM_001354904.1:c.4688C>G	NP_001341833.1:p.Thr1563Ser
NM_001354905.1:c.4586C>G	NP_001341834.1:p.Thr1529Ser
NM_001354906.1:c.4217C>G	NP_001341835.1:p.Thr1406Ser
NM_000038.6:c.5066C>G MANE Select	NP_000029.2:p.Thr1689Ser
NM_001127510.3:c.5066C>G	NP_001120982.1:p.Thr1689Ser
NM_001127511.3:c.5012C>G	NP_001120983.2:p.Thr1671Ser
NM_001354895.2:c.5066C>G	NP_001341824.1:p.Thr1689Ser
NM_001354896.2:c.5120C>G	NP_001341825.1:p.Thr1707Ser
NM_001354897.2:c.5096C>G	NP_001341826.1:p.Thr1699Ser
NM_001354898.2:c.4991C>G	NP_001341827.1:p.Thr1664Ser
NM_001354899.2:c.4982C>G	NP_001341828.1:p.Thr1661Ser
NM_001354900.2:c.4943C>G	NP_001341829.1:p.Thr1648Ser
NM_001354901.2:c.4889C>G	NP_001341830.1:p.Thr1630Ser
NM_001354902.2:c.4793C>G	NP_001341831.1:p.Thr1598Ser
NM_001354903.2:c.4763C>G	NP_001341832.1:p.Thr1588Ser
NM_001354904.2:c.4688C>G	NP_001341833.1:p.Thr1563Ser
NM_001354905.2:c.4586C>G	NP_001341834.1:p.Thr1529Ser
NM_001354906.2:c.4217C>G	NP_001341835.1:p.Thr1406Ser