Canonical Allele Identifier: CA658760636

Gene: APC

Linked Data

• ClinVar Variation Id: 2583444
• ClinVar RCV Id: RCV003337462
• PubMed: PMID:20685668

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112835166del , CM000667.2:g.112835166del	GRCh38
NC_000005.9:g.112170863del , CM000667.1:g.112170863del	GRCh37
NC_000005.8:g.112198762del	NCBI36
NG_008481.4:g.147646del , LRG_130:g.147646del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1623+1del
ENST00000504915.3:c.2012+1del
ENST00000505350.2:c.*1964+1del
ENST00000507379.6:c.1904+1del
ENST00000509732.6:c.1958+1del
ENST00000512211.7:c.1958+1del
ENST00000257430.9:c.1958+1del
ENST00000257430.8:c.1958+1del
ENST00000502371.2:c.311+1del
ENST00000504915.2:c.647+1del
ENST00000507379.5:c.1904+1del
ENST00000508376.6:c.1958+1del
ENST00000508624.5:c.*1280+1del
ENST00000512211.6:c.1958+1del
ENST00000520401.1:c.230+6194del
NM_000038.5:c.1958+1del
NM_001127510.2:c.1958+1del
NM_001127511.2:c.1904+1del
NM_001354895.1:c.1958+1del
NM_001354896.1:c.2012+1del
NM_001354897.1:c.1988+1del
NM_001354898.1:c.1883+1del
NM_001354899.1:c.1874+1del
NM_001354900.1:c.1835+1del
NM_001354901.1:c.1781+1del
NM_001354902.1:c.1685+1del
NM_001354903.1:c.1655+1del
NM_001354904.1:c.1580+1del
NM_001354905.1:c.1478+1del
NM_001354906.1:c.1109+1del
NM_000038.6:c.1958+1del
NM_001127510.3:c.1958+1del
NM_001127511.3:c.1904+1del
NM_001354895.2:c.1958+1del
NM_001354896.2:c.2012+1del
NM_001354897.2:c.1988+1del
NM_001354898.2:c.1883+1del
NM_001354899.2:c.1874+1del
NM_001354900.2:c.1835+1del
NM_001354901.2:c.1781+1del
NM_001354902.2:c.1685+1del
NM_001354903.2:c.1655+1del
NM_001354904.2:c.1580+1del
NM_001354905.2:c.1478+1del
NM_001354906.2:c.1109+1del