Canonical Allele Identifier: CA2573138710

Gene: APC

Linked Data

• ClinVar Variation Id: 1459357
• ClinVar RCV Id: RCV003745458
• dbSNP Id: rs2149924494

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840410del , CM000667.2:g.112840410del	GRCh38
NC_000005.9:g.112176107del , CM000667.1:g.112176107del	GRCh37
NC_000005.8:g.112204006del	NCBI36
NG_008481.4:g.152890del , LRG_130:g.152890del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4870del	ENSP00000473355.2:p.Ala1624GlnfsTer?
ENST00000505350.2:c.*4822del	ENSP00000481752.1:n.*4822del
ENST00000507379.6:c.4762del	ENSP00000423224.2:p.Ala1588GlnfsTer?
ENST00000509732.6:c.4816del	ENSP00000426541.2:p.Ala1606GlnfsTer?
ENST00000512211.7:c.4816del	ENSP00000423828.3:p.Ala1606GlnfsTer?
ENST00000257430.9:c.4816del MANE Select	ENSP00000257430.4:p.Ala1606GlnfsTer?
ENST00000257430.8:c.4816del	ENSP00000257430.4:p.Ala1606GlnfsTer?
ENST00000508376.6:c.4816del	ENSP00000427089.2:p.Ala1606GlnfsTer?
ENST00000508624.5:c.*4138del	ENSP00000424265.1:n.*4138del
ENST00000520401.1:c.230+11438del
NM_000038.5:c.4816del	NP_000029.2:p.Ala1606GlnfsTer?
NM_001127510.2:c.4816del	NP_001120982.1:p.Ala1606GlnfsTer?
NM_001127511.2:c.4762del	NP_001120983.2:p.Ala1588GlnfsTer?
NM_001354895.1:c.4816del	NP_001341824.1:p.Ala1606GlnfsTer?
NM_001354896.1:c.4870del	NP_001341825.1:p.Ala1624GlnfsTer?
NM_001354897.1:c.4846del	NP_001341826.1:p.Ala1616GlnfsTer?
NM_001354898.1:c.4741del	NP_001341827.1:p.Ala1581GlnfsTer?
NM_001354899.1:c.4732del	NP_001341828.1:p.Ala1578GlnfsTer?
NM_001354900.1:c.4693del	NP_001341829.1:p.Ala1565GlnfsTer?
NM_001354901.1:c.4639del	NP_001341830.1:p.Ala1547GlnfsTer?
NM_001354902.1:c.4543del	NP_001341831.1:p.Ala1515GlnfsTer?
NM_001354903.1:c.4513del	NP_001341832.1:p.Ala1505GlnfsTer?
NM_001354904.1:c.4438del	NP_001341833.1:p.Ala1480GlnfsTer?
NM_001354905.1:c.4336del	NP_001341834.1:p.Ala1446GlnfsTer?
NM_001354906.1:c.3967del	NP_001341835.1:p.Ala1323GlnfsTer?
NM_000038.6:c.4816del MANE Select	NP_000029.2:p.Ala1606GlnfsTer?
NM_001127510.3:c.4816del	NP_001120982.1:p.Ala1606GlnfsTer?
NM_001127511.3:c.4762del	NP_001120983.2:p.Ala1588GlnfsTer?
NM_001354895.2:c.4816del	NP_001341824.1:p.Ala1606GlnfsTer?
NM_001354896.2:c.4870del	NP_001341825.1:p.Ala1624GlnfsTer?
NM_001354897.2:c.4846del	NP_001341826.1:p.Ala1616GlnfsTer?
NM_001354898.2:c.4741del	NP_001341827.1:p.Ala1581GlnfsTer?
NM_001354899.2:c.4732del	NP_001341828.1:p.Ala1578GlnfsTer?
NM_001354900.2:c.4693del	NP_001341829.1:p.Ala1565GlnfsTer?
NM_001354901.2:c.4639del	NP_001341830.1:p.Ala1547GlnfsTer?
NM_001354902.2:c.4543del	NP_001341831.1:p.Ala1515GlnfsTer?
NM_001354903.2:c.4513del	NP_001341832.1:p.Ala1505GlnfsTer?
NM_001354904.2:c.4438del	NP_001341833.1:p.Ala1480GlnfsTer?
NM_001354905.2:c.4336del	NP_001341834.1:p.Ala1446GlnfsTer?
NM_001354906.2:c.3967del	NP_001341835.1:p.Ala1323GlnfsTer?