Canonical Allele Identifier: CA658655952

Gene: APC

Linked Data

• ClinVar Variation Id: 486781
• ClinVar RCV Id: RCV000573063
• dbSNP Id: rs1554086182
• MyVariant Identifiers: chr5:g.112176061del (hg19) ; chr5:g.112840364del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840364del , CM000667.2:g.112840364del	GRCh38
NC_000005.9:g.112176061del , CM000667.1:g.112176061del	GRCh37
NC_000005.8:g.112203960del	NCBI36
NG_008481.4:g.152844del , LRG_130:g.152844del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4824del	ENSP00000473355.2:p.Ala1609GlnfsTer?
ENST00000505350.2:c.*4776del	ENSP00000481752.1:n.*4776del
ENST00000507379.6:c.4716del	ENSP00000423224.2:p.Ala1573GlnfsTer?
ENST00000509732.6:c.4770del	ENSP00000426541.2:p.Ala1591GlnfsTer?
ENST00000512211.7:c.4770del	ENSP00000423828.3:p.Ala1591GlnfsTer?
ENST00000257430.9:c.4770del MANE Select	ENSP00000257430.4:p.Ala1591GlnfsTer?
ENST00000257430.8:c.4770del	ENSP00000257430.4:p.Ala1591GlnfsTer?
ENST00000508376.6:c.4770del	ENSP00000427089.2:p.Ala1591GlnfsTer?
ENST00000508624.5:c.*4092del	ENSP00000424265.1:n.*4092del
ENST00000520401.1:c.230+11392del
NM_000038.5:c.4770del	NP_000029.2:p.Ala1591GlnfsTer?
NM_001127510.2:c.4770del	NP_001120982.1:p.Ala1591GlnfsTer?
NM_001127511.2:c.4716del	NP_001120983.2:p.Ala1573GlnfsTer?
NM_001354895.1:c.4770del	NP_001341824.1:p.Ala1591GlnfsTer?
NM_001354896.1:c.4824del	NP_001341825.1:p.Ala1609GlnfsTer?
NM_001354897.1:c.4800del	NP_001341826.1:p.Ala1601GlnfsTer?
NM_001354898.1:c.4695del	NP_001341827.1:p.Ala1566GlnfsTer?
NM_001354899.1:c.4686del	NP_001341828.1:p.Ala1563GlnfsTer?
NM_001354900.1:c.4647del	NP_001341829.1:p.Ala1550GlnfsTer?
NM_001354901.1:c.4593del	NP_001341830.1:p.Ala1532GlnfsTer?
NM_001354902.1:c.4497del	NP_001341831.1:p.Ala1500GlnfsTer?
NM_001354903.1:c.4467del	NP_001341832.1:p.Ala1490GlnfsTer?
NM_001354904.1:c.4392del	NP_001341833.1:p.Ala1465GlnfsTer?
NM_001354905.1:c.4290del	NP_001341834.1:p.Ala1431GlnfsTer?
NM_001354906.1:c.3921del	NP_001341835.1:p.Ala1308GlnfsTer?
NM_000038.6:c.4770del MANE Select	NP_000029.2:p.Ala1591GlnfsTer?
NM_001127510.3:c.4770del	NP_001120982.1:p.Ala1591GlnfsTer?
NM_001127511.3:c.4716del	NP_001120983.2:p.Ala1573GlnfsTer?
NM_001354895.2:c.4770del	NP_001341824.1:p.Ala1591GlnfsTer?
NM_001354896.2:c.4824del	NP_001341825.1:p.Ala1609GlnfsTer?
NM_001354897.2:c.4800del	NP_001341826.1:p.Ala1601GlnfsTer?
NM_001354898.2:c.4695del	NP_001341827.1:p.Ala1566GlnfsTer?
NM_001354899.2:c.4686del	NP_001341828.1:p.Ala1563GlnfsTer?
NM_001354900.2:c.4647del	NP_001341829.1:p.Ala1550GlnfsTer?
NM_001354901.2:c.4593del	NP_001341830.1:p.Ala1532GlnfsTer?
NM_001354902.2:c.4497del	NP_001341831.1:p.Ala1500GlnfsTer?
NM_001354903.2:c.4467del	NP_001341832.1:p.Ala1490GlnfsTer?
NM_001354904.2:c.4392del	NP_001341833.1:p.Ala1465GlnfsTer?
NM_001354905.2:c.4290del	NP_001341834.1:p.Ala1431GlnfsTer?
NM_001354906.2:c.3921del	NP_001341835.1:p.Ala1308GlnfsTer?