Canonical Allele Identifier: CA658683034

Gene: APC

Linked Data

• ClinVar Variation Id: 633040
• ClinVar RCV Id: RCV000780852 ; RCV002422669 ; RCV001354694
• dbSNP Id: rs1561569606

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112835166_112835167dup , CM000667.2:g.112835166_112835167dup	GRCh38
NC_000005.9:g.112170863_112170864dup , CM000667.1:g.112170863_112170864dup	GRCh37
NC_000005.8:g.112198762_112198763dup	NCBI36
NG_008481.4:g.147646_147647dup , LRG_130:g.147646_147647dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1623+1_1623+2dup	ENSP00000484935.2:n.1623+1_1623+2dup
ENST00000504915.3:c.2012+1_2012+2dup	ENSP00000473355.2:n.2012+1_2012+2dup
ENST00000505350.2:c.*1964+1_*1964+2dup	ENSP00000481752.1:n.*1964+1_*1964+2dup
ENST00000507379.6:c.1904+1_1904+2dup	ENSP00000423224.2:n.1904+1_1904+2dup
ENST00000509732.6:c.1958+1_1958+2dup	ENSP00000426541.2:n.1958+1_1958+2dup
ENST00000512211.7:c.1958+1_1958+2dup	ENSP00000423828.3:n.1958+1_1958+2dup
ENST00000257430.9:c.1958+1_1958+2dup MANE Select	ENSP00000257430.4:n.1958+1_1958+2dup
ENST00000257430.8:c.1958+1_1958+2dup	ENSP00000257430.4:n.1958+1_1958+2dup
ENST00000502371.2:c.311+1_311+2dup
ENST00000504915.2:c.647+1_647+2dup	ENSP00000473355.1:n.647+1_647+2dup
ENST00000507379.5:c.1904+1_1904+2dup	ENSP00000423224.1:n.1904+1_1904+2dup
ENST00000508376.6:c.1958+1_1958+2dup	ENSP00000427089.2:n.1958+1_1958+2dup
ENST00000508624.5:c.*1280+1_*1280+2dup	ENSP00000424265.1:n.*1280+1_*1280+2dup
ENST00000512211.6:c.1958+1_1958+2dup	ENSP00000423828.2:n.1958+1_1958+2dup
ENST00000520401.1:c.230+6194_230+6195dup
NM_000038.5:c.1958+1_1958+2dup	NP_000029.2:n.1958+1_1958+2dup
NM_001127510.2:c.1958+1_1958+2dup	NP_001120982.1:n.1958+1_1958+2dup
NM_001127511.2:c.1904+1_1904+2dup	NP_001120983.2:n.1904+1_1904+2dup
NM_001354895.1:c.1958+1_1958+2dup	NP_001341824.1:n.1958+1_1958+2dup
NM_001354896.1:c.2012+1_2012+2dup	NP_001341825.1:n.2012+1_2012+2dup
NM_001354897.1:c.1988+1_1988+2dup	NP_001341826.1:n.1988+1_1988+2dup
NM_001354898.1:c.1883+1_1883+2dup	NP_001341827.1:n.1883+1_1883+2dup
NM_001354899.1:c.1874+1_1874+2dup	NP_001341828.1:n.1874+1_1874+2dup
NM_001354900.1:c.1835+1_1835+2dup	NP_001341829.1:n.1835+1_1835+2dup
NM_001354901.1:c.1781+1_1781+2dup	NP_001341830.1:n.1781+1_1781+2dup
NM_001354902.1:c.1685+1_1685+2dup	NP_001341831.1:n.1685+1_1685+2dup
NM_001354903.1:c.1655+1_1655+2dup	NP_001341832.1:n.1655+1_1655+2dup
NM_001354904.1:c.1580+1_1580+2dup	NP_001341833.1:n.1580+1_1580+2dup
NM_001354905.1:c.1478+1_1478+2dup	NP_001341834.1:n.1478+1_1478+2dup
NM_001354906.1:c.1109+1_1109+2dup	NP_001341835.1:n.1109+1_1109+2dup
NM_000038.6:c.1958+1_1958+2dup MANE Select	NP_000029.2:n.1958+1_1958+2dup
NM_001127510.3:c.1958+1_1958+2dup	NP_001120982.1:n.1958+1_1958+2dup
NM_001127511.3:c.1904+1_1904+2dup	NP_001120983.2:n.1904+1_1904+2dup
NM_001354895.2:c.1958+1_1958+2dup	NP_001341824.1:n.1958+1_1958+2dup
NM_001354896.2:c.2012+1_2012+2dup	NP_001341825.1:n.2012+1_2012+2dup
NM_001354897.2:c.1988+1_1988+2dup	NP_001341826.1:n.1988+1_1988+2dup
NM_001354898.2:c.1883+1_1883+2dup	NP_001341827.1:n.1883+1_1883+2dup
NM_001354899.2:c.1874+1_1874+2dup	NP_001341828.1:n.1874+1_1874+2dup
NM_001354900.2:c.1835+1_1835+2dup	NP_001341829.1:n.1835+1_1835+2dup
NM_001354901.2:c.1781+1_1781+2dup	NP_001341830.1:n.1781+1_1781+2dup
NM_001354902.2:c.1685+1_1685+2dup	NP_001341831.1:n.1685+1_1685+2dup
NM_001354903.2:c.1655+1_1655+2dup	NP_001341832.1:n.1655+1_1655+2dup
NM_001354904.2:c.1580+1_1580+2dup	NP_001341833.1:n.1580+1_1580+2dup
NM_001354905.2:c.1478+1_1478+2dup	NP_001341834.1:n.1478+1_1478+2dup
NM_001354906.2:c.1109+1_1109+2dup	NP_001341835.1:n.1109+1_1109+2dup