Canonical Allele Identifier: CA16024927

Gene: APC

Linked Data

• ClinVar Variation Id: 568451
• ClinVar RCV Id: RCV003534576 ; RCV004004287
• dbSNP Id: rs1561557447
• gnomAD v3: 5-112828884-C-G
• gnomAD v4: 5-112828884-C-G
• MyVariant Identifiers: chr5:g.112164581C>G (hg19) ; chr5:g.112828884C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1409-6067C>G	ENSP00000484935.2:n.1409-6067C>G
ENST00000504915.3:c.1709C>G	ENSP00000473355.2:p.Ser570Cys
ENST00000505084.2:n.1711C>G
ENST00000505350.2:c.*1661C>G	ENSP00000481752.1:n.*1661C>G
ENST00000507379.6:c.1601C>G	ENSP00000423224.2:p.Ser534Cys
ENST00000509732.6:c.1655C>G	ENSP00000426541.2:p.Ser552Cys
ENST00000512211.7:c.1655C>G	ENSP00000423828.3:p.Ser552Cys
ENST00000257430.9:c.1655C>G MANE Select	ENSP00000257430.4:p.Ser552Cys
ENST00000257430.8:c.1655C>G	ENSP00000257430.4:p.Ser552Cys
ENST00000502371.2:c.97-6067C>G
ENST00000504915.2:c.344C>G	ENSP00000473355.1:p.Ser115Cys
ENST00000505084.1:n.142C>G
ENST00000507379.5:c.1601C>G	ENSP00000423224.1:p.Ser534Cys
ENST00000508376.6:c.1655C>G	ENSP00000427089.2:p.Ser552Cys
ENST00000508624.5:c.*977C>G	ENSP00000424265.1:n.*977C>G
ENST00000512211.6:c.1655C>G	ENSP00000423828.2:p.Ser552Cys
ENST00000520401.1:c.142C>G
NM_000038.5:c.1655C>G	NP_000029.2:p.Ser552Cys
NM_001127510.2:c.1655C>G	NP_001120982.1:p.Ser552Cys
NM_001127511.2:c.1601C>G	NP_001120983.2:p.Ser534Cys
NM_001354895.1:c.1655C>G	NP_001341824.1:p.Ser552Cys
NM_001354896.1:c.1709C>G	NP_001341825.1:p.Ser570Cys
NM_001354897.1:c.1685C>G	NP_001341826.1:p.Ser562Cys
NM_001354898.1:c.1580C>G	NP_001341827.1:p.Ser527Cys
NM_001354899.1:c.1571C>G	NP_001341828.1:p.Ser524Cys
NM_001354900.1:c.1532C>G	NP_001341829.1:p.Ser511Cys
NM_001354901.1:c.1478C>G	NP_001341830.1:p.Ser493Cys
NM_001354902.1:c.1382C>G	NP_001341831.1:p.Ser461Cys
NM_001354903.1:c.1352C>G	NP_001341832.1:p.Ser451Cys
NM_001354904.1:c.1277C>G	NP_001341833.1:p.Ser426Cys
NM_001354905.1:c.1175C>G	NP_001341834.1:p.Ser392Cys
NM_001354906.1:c.806C>G	NP_001341835.1:p.Ser269Cys
NM_000038.6:c.1655C>G MANE Select	NP_000029.2:p.Ser552Cys
NM_001127510.3:c.1655C>G	NP_001120982.1:p.Ser552Cys
NM_001127511.3:c.1601C>G	NP_001120983.2:p.Ser534Cys
NM_001354895.2:c.1655C>G	NP_001341824.1:p.Ser552Cys
NM_001354896.2:c.1709C>G	NP_001341825.1:p.Ser570Cys
NM_001354897.2:c.1685C>G	NP_001341826.1:p.Ser562Cys
NM_001354898.2:c.1580C>G	NP_001341827.1:p.Ser527Cys
NM_001354899.2:c.1571C>G	NP_001341828.1:p.Ser524Cys
NM_001354900.2:c.1532C>G	NP_001341829.1:p.Ser511Cys
NM_001354901.2:c.1478C>G	NP_001341830.1:p.Ser493Cys
NM_001354902.2:c.1382C>G	NP_001341831.1:p.Ser461Cys
NM_001354903.2:c.1352C>G	NP_001341832.1:p.Ser451Cys
NM_001354904.2:c.1277C>G	NP_001341833.1:p.Ser426Cys
NM_001354905.2:c.1175C>G	NP_001341834.1:p.Ser392Cys
NM_001354906.2:c.806C>G	NP_001341835.1:p.Ser269Cys