Canonical Allele Identifier: CA16024926

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112164581C>A (hg19) ; chr5:g.112828884C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112828884C>A , CM000667.2:g.112828884C>A	GRCh38
NC_000005.9:g.112164581C>A , CM000667.1:g.112164581C>A	GRCh37
NC_000005.8:g.112192480C>A	NCBI36
NG_008481.4:g.141364C>A , LRG_130:g.141364C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1409-6067C>A	ENSP00000484935.2:n.1409-6067C>A
ENST00000504915.3:c.1709C>A	ENSP00000473355.2:p.Ser570Tyr
ENST00000505084.2:n.1711C>A
ENST00000505350.2:c.*1661C>A	ENSP00000481752.1:n.*1661C>A
ENST00000507379.6:c.1601C>A	ENSP00000423224.2:p.Ser534Tyr
ENST00000509732.6:c.1655C>A	ENSP00000426541.2:p.Ser552Tyr
ENST00000512211.7:c.1655C>A	ENSP00000423828.3:p.Ser552Tyr
ENST00000257430.9:c.1655C>A MANE Select	ENSP00000257430.4:p.Ser552Tyr
ENST00000257430.8:c.1655C>A	ENSP00000257430.4:p.Ser552Tyr
ENST00000502371.2:c.97-6067C>A
ENST00000504915.2:c.344C>A	ENSP00000473355.1:p.Ser115Tyr
ENST00000505084.1:n.142C>A
ENST00000507379.5:c.1601C>A	ENSP00000423224.1:p.Ser534Tyr
ENST00000508376.6:c.1655C>A	ENSP00000427089.2:p.Ser552Tyr
ENST00000508624.5:c.*977C>A	ENSP00000424265.1:n.*977C>A
ENST00000512211.6:c.1655C>A	ENSP00000423828.2:p.Ser552Tyr
ENST00000520401.1:c.142C>A
NM_000038.5:c.1655C>A	NP_000029.2:p.Ser552Tyr
NM_001127510.2:c.1655C>A	NP_001120982.1:p.Ser552Tyr
NM_001127511.2:c.1601C>A	NP_001120983.2:p.Ser534Tyr
NM_001354895.1:c.1655C>A	NP_001341824.1:p.Ser552Tyr
NM_001354896.1:c.1709C>A	NP_001341825.1:p.Ser570Tyr
NM_001354897.1:c.1685C>A	NP_001341826.1:p.Ser562Tyr
NM_001354898.1:c.1580C>A	NP_001341827.1:p.Ser527Tyr
NM_001354899.1:c.1571C>A	NP_001341828.1:p.Ser524Tyr
NM_001354900.1:c.1532C>A	NP_001341829.1:p.Ser511Tyr
NM_001354901.1:c.1478C>A	NP_001341830.1:p.Ser493Tyr
NM_001354902.1:c.1382C>A	NP_001341831.1:p.Ser461Tyr
NM_001354903.1:c.1352C>A	NP_001341832.1:p.Ser451Tyr
NM_001354904.1:c.1277C>A	NP_001341833.1:p.Ser426Tyr
NM_001354905.1:c.1175C>A	NP_001341834.1:p.Ser392Tyr
NM_001354906.1:c.806C>A	NP_001341835.1:p.Ser269Tyr
NM_000038.6:c.1655C>A MANE Select	NP_000029.2:p.Ser552Tyr
NM_001127510.3:c.1655C>A	NP_001120982.1:p.Ser552Tyr
NM_001127511.3:c.1601C>A	NP_001120983.2:p.Ser534Tyr
NM_001354895.2:c.1655C>A	NP_001341824.1:p.Ser552Tyr
NM_001354896.2:c.1709C>A	NP_001341825.1:p.Ser570Tyr
NM_001354897.2:c.1685C>A	NP_001341826.1:p.Ser562Tyr
NM_001354898.2:c.1580C>A	NP_001341827.1:p.Ser527Tyr
NM_001354899.2:c.1571C>A	NP_001341828.1:p.Ser524Tyr
NM_001354900.2:c.1532C>A	NP_001341829.1:p.Ser511Tyr
NM_001354901.2:c.1478C>A	NP_001341830.1:p.Ser493Tyr
NM_001354902.2:c.1382C>A	NP_001341831.1:p.Ser461Tyr
NM_001354903.2:c.1352C>A	NP_001341832.1:p.Ser451Tyr
NM_001354904.2:c.1277C>A	NP_001341833.1:p.Ser426Tyr
NM_001354905.2:c.1175C>A	NP_001341834.1:p.Ser392Tyr
NM_001354906.2:c.806C>A	NP_001341835.1:p.Ser269Tyr